Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
  • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
  • A61P31/14—Antivirals for RNA viruses
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
  • C07D209/04—Indoles; Hydrogenated indoles
  • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
  • C07D209/04—Indoles; Hydrogenated indoles
  • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
  • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
  • C07D513/04—Ortho-condensed systems

Definitions

• the invention relates to inhibitors of RNA.dependent RNA polymerases, particularly those, viral polymerases within the Flaviviridae family, more particularly to HCV polymerase.
• HCV hepatitis C virus
• HCV-associated end-stage liver disease is now the leading cause of liver transplantation.
• hepatitis C is responsible for 8,000 to 10,000 deaths annually. Without effective intervention, the number is expected to triple in the next 10 to 20 years.
• Prolonged treatment of chronically infected patients with interferon or interferon and ribavjrin is the only currently approved therapy, but it achieves a sustained response in fewer than 50% of cases (Lindsay, K.L.; 1997; Hepatology 26: 71 S-77S*, and Reichard, O.; Schvarcz, R.; Weiland, O.; 1997 Hepatology 26: 108S-111S*).
• HCV belongs to the family Flaviviridae, genus hepacivirus, which comprises three genera of small enveloped positive-strand RNA viruses (Rice, CM.; 1996; "Flaviviridae: the viruses and their replication"; pp. 931-960 in Fields Virology; Fields, B.N.; Knipe, D.M.; Howley, P.M. (eds.); Lippincott-Raven Publishers, Philadelphia Pa. *).
• the 9.6 kb genome of HCV consists of a long open reading frame (ORF) flanked by 5' and 3' non-translated regions (NTR's).
• the HCV 5' NTR is 341 nucleotides in length and functions as an internal ribosome entry site for cap- independent translation initiation (Lemon, S.H.; Honda, M.; 1997; Semin. Virol. 8: 274-288).
• the HCV polyprotein is cleaved co- and post-translationally into at least 10 individual polypeptides (Reed, K.E.; Rice, CM.; 1999; Curr. Top. Microbiol. Immunol. 242: 55-84*).
• the structural proteins result from signal peptidases in the N- terminal portion of the polyprotein. Two viral proteases mediate downstream cleavages to produce non-structural (NS) proteins that function as components of the HCV RNA replicase.
• NS non-structural
• the NS2-3 protease spans the C-terminal half of the NS2 and the N-terminal one-third of NS3 and catalyses cis cleavage of the NS2/3 site.
• the same portion of NS3 also encodes the catalytic domain of the NS3-4A serine protease that cleaves at four downstream sites.
• the C-terminal two-thirds of NS3 is highly conserved amongst HCV isolates, with RNA-binding, RNA-stimulated NTPase, and RNA unwinding activities.
• NS4B and the NS5A phosphoprotein are also likely components of the replicase, their specific roles are unknown.
• the C-terminal polyprotein cleavage product, NS5B is the elongation subunit of the HCV replicase possessing RNA-dependent RNA polymerase (RdRp) activity (Behrens, S.E.; Tomei, L; DeFrancesco, R.; 1996; EMBO J. 15: 12-22*; and Lohmann, V.; K ⁇ rner, F.; Herian, U.; Bartenschlager, R.; 1997; J. Virol. 71: 8416- 8428*).
• RdRp RNA-dependent RNA polymerase
• RNA dependent RNA polymerases in mammals, and the fact that this enzyme appears to be essential to viral replication, would suggest that the NS5B polymerase is an ideal target for anti-HCV therapeutics.
• WO 00/06529, WO 00/13708, WO 00/10573, WO 00/18231, WO 01/47883, WO 01/85172 and WO 02/04425 report inhibitors of NS5B proposed for treatment of HCV.
• a or B is N and the other B or A is C, wherein — between two C-atoms represents a double bond and — between a C-atom and a N-atom represents a single bond,
• M 4 is CR 4 4 b D ,
• Sp is a spacer group selected from -(CR 51 R 52 ) k ⁇ -, wherein k1 is 1 , 2 or 3;
• R 51 , R 52 are independently H, (C*,- 6 )alkyl, (C 3 - )cycloalkyl or (C 1 - 3 )alkyl-
• R 51 and R 52 are covalently bonded together and to the carbon-atom to which they are attached to form a 3, 4, 5, 6 or 7-membered saturated or 5, 6 or 7- membered unsaturated cyclic system whereby the 5, 6 or 7-membered saturated or unsaturated cyclic system optionally contains 1 to 3 heteroatoms .
• selected from N, O or S said alkyl, cycloalkyl, alkyl-cycloalkyl or cyclic system being optionally substituted by halogen, hydroxy, (C 1 - 6 )alkoxy, cyano, amino, -NH C- M -alkyl) and/or ⁇ (d ⁇ -alky a;
• Y° is O, S, NR 11 or CR 12 R 13 , wherein
• R 11 , R 12 , R 13 are each independently defined as R°; R 3 may also be COOR° or SO 2 R c ; wherein R c and each R° is optionally substituted with R 150 ;
• R 12 and R 13 are covalently bonded together and to the carbon-atom to which they are attached to form a 3, 4, 5, 6 or 7-membered saturated or 5, 6 or 7-membered unsaturated cyclic system whereby the 5, 6 or 7-membered saturated or unsaturated cyclic system may contain 1 to 3 heteroatoms selected from N, O or S; said cyclic systems being optionally substituted with R 150 ;
• L is C ⁇ - 6 alkyl, (C 3 . 6 )cycloalkyl, C 1 . 6 alkyl-(C 3 - 6 )cycloalkyl, (C 2 . 6 )alkenyl, aryl,
• Y° and L are covalently bonded to form a 5, 6, 7 or 8-membered mono- or a 8, 9, 10 or 11 -membered bicyclic group which is optionally unsaturated or aromatic and which optionally contains 1 , 2 or 3 heteroatoms selected from N, O and S, wherein the mono- or bicyclic group is optionally substituted with R 60 ;
• L may also be H; or if Y ⁇ 0 u ; is.. ⁇ the ⁇ n L may also be OR ⁇ , wherein R c is optionally substituted with R 60 ;
• L may also be N(R N2 )R N ⁇ NR N3 -N(R N2 )R Ni , NR N3 -NR N2 -CO-R c , NR N4 -NR N3 -CO-N(R N2 )R N1 , NR N2 -SO 2 -R c ,
• R N1 including any heterocycle or heterobicycle formed by R N1 , R N2 and/or R N3 , and R c and R° being optionally substituted with R 60 ;
• L may also be OR 6a or N(R 5a )R 6a , wherein R Sa is defined as R N2 ,
• R 6a is:
• R 6a is:
• R 7a and R 8a are each independently defined as R°, COOR 0 or CON(R N2 )R N1 , wherein said R° is optionally substituted with R 60 ; or
• R 7a and R 8a are covalently bonded together to form a (C 3 . 7 )cycloalkyl or a 4, 5- or 6-membered heterocycle having from 1 to 3 heteroatom selected from O, N, and S; and when L is N(R 5a )R 6a , either of R 7a or R 8a may be covalently bonded to R 5a to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said cycloalkyl or heterocycle being optionally substituted by R 150 ; and
• alkylene and alkenylene groups according to b), c) and d) may be substituted with (C ⁇ ) alkyl;
• Y 2 is O or S
• R 9a is defined as R°, wherein said R° is optionally substituted with R 60 ; or R 9a is covalently bonded to either of R 7a or R 8a to form a 5- or 6-membered heterocycle;
• Q 1 is aryl, Het, (C*,. 6 )alkyl-aryl, (C ⁇ ) alkyl-Het, (C 1 . 6 )alkyl-CONH-aryl or (C**. 6 ) alkyl-CONH-Het, all of which being optionally substituted with R 60 ;
• Y 1 is O, S or NR 14 , wherein R 14 is H or (C,. ⁇ ) alkyl;
• Z is defined as a) OR 0 ; b) SO 2 R c ; c) N(R N2 )R N1 ; d) NR N3 -N(R N2 )R N1 ; e) NR N3 -NR N2 -CO-R c ; f) NR N -NR N3 -CO-N(R N2 )R N1 ; g) NR N2 -SO 2 -R c or h) NR N3 -SO 2 -N(R N2 )R N1 ; i) NR N2 -CO-R c ; j) COOR 0 ; k) N(R N1 )OR°; wherein R° and R c are optionally substituted with R 60 ; and said R N ⁇ including any heterocycle or heterobicycle formed by R N1 , R N2 , and/or R N3 , being optionally substituted with R 60 ;
• Z is OR 6 or N(R 5 )R 6b wherein R 5b is defined as R N2 and R 6b is: or R bD is
• R 7 , R 8 , Y 3 , R 9b , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively;
• Q 2 is aryl, Het, (d- ⁇ alkyl-aryl, (C- ⁇ alkyl-Het, (C*,. 6 )alkyl-CONH-aryl or (C ⁇ - 6 ) alkyl-CONH-Het, all of which being optionally substituted with R 60 or Q 2 is R 160 or Q 2 is selected from the group consisting of O-C ⁇ -alkyl, S-C ⁇ -alkyl, C 1-4 - alkyl, C 2 - 4 -alkenyl and C 2 ⁇ -alkynyl, all of which being optionally substituted with R 160 ; and
• R 2 is selected from: halogen or R 21 , wherein R 21 is aryl or Het, said R 21 is optionally substituted with R 150 ;
• R 3 is selected from (Chalky!, (C 3 _ 7 )cycloalkyl, (C*,. 3 )alkyl-(C 3 - 7 )cycloalkyl,
• HCy is a saturated or unsaturated 4 to 7-membered heterocyclic group with 1 to 3 heteroatoms selected from O, " S and N; " said alkyl, cycloalkyl, cycloalkenyl, bicycloalkyl, bicycloalkenyl, HCy and alkyl-HCy being optionally substituted with from 1 to 4 substituents selected from: a) halogen; b) (C* ⁇ - 6 )alkyl optionally substituted with:
• R 31 is H, (C* ⁇ - 6 alkyl), (C 3 . 7 )cycloalkyi or (C 1 - 3 )alkyl-(C 3 - 7 )cycloalkyl; or - N(R 32 ) 2 wherein each R 32 is independently H, (C ⁇ - 6 )alkyl, (C 3 - 7 )cycloalkyl or (C*]- 3 )alkyl-(C3- 7 )cycloalkyl; or both R 32 are covalently bonded together and to the nitrogen to which they are attached to form a 5, 6 or 7-membered saturated heterocycle; c) OR 33 or SR 33 wherein R 33 is H, (C*,. 6 )alkyl, (C - 7 )cycloalkyl or
• each R 35 is independently H, (C* ⁇ . 6 )alkyl, (C 3 - 7 )cycloalkyl or (C 1 . 3 )alkyl-(C 3 - 7 )cycloalkyl; or both R 35 are covalently, bonded together and to the nitrogen to which they are attached to form a 5, 6 or 7-membered saturated heterocycle;
• R 4a , R 4b , R 5 each are independently H or defined as R 150 ;
• R 60 is each defined as 1 to 4 substituents independently selected from: - 1 to 3 substituents selected from halogen;
• R N1 , R c and/or R° are optionally substituted with R 160 as defined;
• ,160 is each defined as 1 , 2 or 3 substituents independently selected from: - 1 , 2 or 3 fluorine substituents;
• OR 161 OCF 3l N(R 62 ) 2 , SO 2 N(R 162 ) 2 , NR 162 SO 2 R c , NR 162 COR 162 , CON(R 162 ) 2 , -NR 161 -CO-COOR 161 , -NR 161 -CO-CO(NR 162 ) 2 , -CONR 161 SO 2 R c , CONR 161 - SO 2 N(R 162 ) 2 or -SO 2 -NR 61 -COR c , wherein R 6 , R 163 and each R 162 is independently (d ⁇ Jalkyl, (C 3 . 7 )cycloalkyl or (C 1 .
• R 161 and each R 162 may each independently also be H; or both R 162 are covalently bonded together and to the nitrogen to which they are attached to form a 5, 6 or 7-membered saturated heterocycle;
• R° R c are independently defined as (C ⁇ . 6 )alkyl, (C 3 - 6 )cycloalkyl,
• R N1 is independently selected from H, (d- 6 )alkyl, (C 3 . 7 )cycloalkyl, . (C 3 - 6 )cycloalkyl, (C 2 - 6 )alkenyl, aryl, Het, (C ⁇ Jalkyl-aryl, (C ⁇ * )alkyl-Het; or
• R N2 , R N3 , R N4 are independently H, CH 3 , (C 2 - ⁇ )alkyl, (C 3 . 6 )cycloalkyl, (d. 4 )alkyl-
• (C 3 . 6 )cycloalkyl wherein said alkyl, cycloalkyl or alkylcycloalkyl is optionally substituted with hydroxy, halogen, carboxy, C ⁇ - 6 -alkoxycarbonyl, C ⁇ -alkyl, C* ⁇ . 6 -alkoxy, amino, -NH(C 1 - 4 -alkyl) and/or -N(d- 4 -alkyl) 2 ; and wherein said
• CH 3 is optionally substituted with halogen, carboxy or C ⁇ - 6 -alkoxycarbonyl
• a) of a group N(R N2 )R N1 the substituents R N2 and R N1 ; or b) of a group NR N3 -N(R N2 )R N1 the substituents R N3 and R N1 , or R N2 and R N1 ; may be covalently bonded together to form a 4-, 5-, 6- or 7-membered saturated or unsaturated N-containing heterocycle or a 8-, 9-, 10- or 11- membered N-containing heterobicycle each may have additionally from 1 to 3 heteroatoms selected from O, N, and S;
• Het is defined as a 4-, 5-, 6- or 7-membered heterocycle having 1 to 4 heteroatoms selected from O, N and S, or a 8-, 9-, 10- or 11 -membered heterobicycle having 1 to 5 heteroatoms selected from O, N and S;
• the compounds according to this invention generally show a good to very good inhibitory activity against HCV polymerase.
• compounds according to this invention inhibit RNA synthesis by the RNA dependent RNA polymerase of HCV, especially of the enzyme NS5B encoded by HCV.
• a further advantage of compounds provided by this invention is their low to very low or even non-significant activity against other polymerases.
• a compound of the formula I according to this invention or a pharmaceutically acceptable salt thereof, as an inhibitor of RNA dependent RNA polymerase activity of the enzyme NS5B, encoded by HCV.
• a compound of the formula I according to this invention or a pharmaceutically acceptable salt thereof, as an inhibitor of HCV replication.
• a method of treating or preventing HCV infection in a mammal comprising administe ⁇ ng to the mammal an effective amount of a compound of formula I according to this invention, or a pharmaceutically acceptable salt thereof .
• a method of treating or preventing HCV infection in a mammal comprising administering to the mammal an effective amount of a compound of formula I, or a pharmaceutically acceptable salt thereof in combination with another antiviral agent.
• a pharmaceutical composition for the treatment or prevention of HCV infection comprising an effective amount of a compound of formula I according to this invention, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
• the pharmaceutical compositions of this invention comprise a therapeutically effective amount of one or more antiviral agents.
• antiviral agents include, ribavirin and amantadine.
• compositions of this invention comprise an other anti-HCV agent as an antiviral agent.
• the pharmaceutical compositions of this invention comprise an additional immunomodulatory agent as an other anti-HCV agent.
• additional immunomodulatory agents include but are not limited to, ⁇ -, ⁇ -, ⁇ - ⁇ -, tau- and ⁇ -interferons.
• compositions of this invention comprise another inhibitor of HCV polymerase as an other anti-HCV agent.
• compositions of this invention comprise an inhibitor of HCV NS3 protease as an other anti-HCV agent.
• compositions of this invention comprise an inhibitor of another target in the HCV life cycle as an other anti-HCV agent.
• examples of such other targets are HCV helicase, HCV NS2/3 protease or HCV IRES.
• a compound of formula I according to this invention for the manufacture of a medicament for the treatment and/or the prevention of a Flaviviridae viral infection, preferably an HCV infection.
• X . is CI, Br or l.
• a twelfth aspect of this invention is related to a process for producing compounds of formula 1.1
• R° and R 3 are defined as hereinbefore and X is Cl, Br or I; according to one of the following methods a), b), c) or d): 1.) cross-coupling of the indole derivative of the formula 2(iv) with an organometallic species such as, but not limited to i) a stannane derivative of the formula R 2 -SnR' 3 , wherein R 2 is defined as hereinbefore and R' is a d.
• organometallic species such as, but not limited to i) a stannane derivative of the formula R 2 -SnR' 3 , wherein R 2 is defined as hereinbefore and R' is a d.
• R , R and R are defined as hereinbefore;
• Y° and L are as defined hereinbefore, in the presence of a strong base, yielding the product of the formula 1.1 ;
• the term (d. n ) alkyl or Ci- n -alkyl, wherein n is an integer, either alone or in combination with another radical, are intended to mean acyclic straight or branched chain alkyl radicals containing 1 to n carbon atoms respectively.
• examples of such radicals include methyl, ethyl, n-propyl, 1-methylethy! (i-propyl), n-butyl, 1- - methylpropyl, 2-methylpropyl, 1 ,1-dimethylethyl (tert-butyl), n-pentyl, etc.
• Me denotes a methyl group.
• alkyl group is substituted by halogen, it is preferably mono-, di- or trisubstituted with fluorine or monosubstituted by chlorine or bromine.
• Preferred alkyl-groups which are trisubstituted with fluorine have a terminal CF 3 group.
• (C 2 . ⁇ ) alkenyl wherein n is an integer, either alone or in combination with another radical, is intended to mean an unsaturated, acyclic straight chain radical containing two to n carbon atoms, at least two of which are bonded to each other by a double bond.
• examples of such radicals are ethenyl (vinyl), 1-propenyl, 2- ⁇ ropenyl, 1-butenyl, etc..
• (C 2 . n ) alkynyl wherein n is an integer, either alone or in combination with another group, is intended to mean an unsaturated, acyclic straight chain radical containing 2 to n carbon atoms, at least two of which are bonded to each other by a triple bond.
• examples of such radicals are ethynyl, 1-propynyl, 2- propynyl, etc.
• (C 3 . n )cycloalkyl wherein n is an integer, either alone or in combination with another radical, means a cycloalkyl radical containing from three to n carbon atoms and includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl.
• (C . n )cycloalkenyl wherein n is an integer, either alone or in combination with another radical, means an unsaturated cyclic radical containing five to n carbon atoms. Examples are cyclopentenyl and cyclohexenyl.
• (C*i- n )alkyl-(C 3 - m )cycloalkyl wherein n and m are integers, either alone or in combination with another radical, means a branched or straight chain alkyl radical having 1 to n C-atoms to which a cycloalkyl radical containing from three to m C-atoms is covalently bonded.
• the alkyl radical is a straight chain and the cycloalkyl radical is linked to its terminal C-atom.
• Examples of (C 1 - 3 )alkyl-(C 3 . 6 )cycloalkyl include cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 2-cyclopropylethyl, 2-cyclobutylethyl, 2-cyclopentylethyl, 2-cyclohexylethyl, 3-cyclopropylpropyl, 3-cyclobutylpropyl, 3-cyclopentylpropyl, 3-cyclohexylpropyl, etc..
• alkyl-aryl, alkyl-HCy, alkyl-Hetaryl, alkyl-Het, etc. mean an alkyl radical to which an aryl, HCy, Hetaryl, Het group is bonded, respectively.
• Examples of (C**. 3 )alkyl ⁇ ary! are benzyl (phenylmethyl), phenylethyl and phenylpropyl.
• CPG carboxy protecting group
• A-carboxyl group is usually protected as an ester that can be cleaved to give the carboxylic acid.
• Protecting groups that can be used include: 1) alkyl esters such as methyl, trimethylsilylethyl and f-butyl, 2) aralkyl esters such as benzyl and substituted benzyl, or 3) esters that can be cleaved by mild base treatment or mild reductive means such as trichloroethyl and phenacyl esters.
• aryl either alone or in combination with another radical means a 6- or 10-membered aryl, i.e. an aromatic radical containing six or ten carbon atoms, for example phenyl, 1 -naphthyl or 2-naphthyl. The most preferred meaning of aryl is phenyl.
• heteroatom means O, S or N.
• heterocycle either alone or in combination with another radical, means a monovalent radical derived by removal of a hydrogen from a four-, five-, six-, or seven-membered saturated or unsaturated (including aromatic) heterocycle containing from one to four heteroatoms selected from nitrogen, oxygen and sulfur.
• heterocycles include, but are not limited to, azetidine, pyrrolidine, tetrahydrofuran, thiazolidine, pyrrole, thiophene, hydantoin, diazepine, 1 H-imidazole, isoxazole, thiazole, tetrazole, piperidine, piperazine, h ⁇ mopiperidine, homopiperazine, 1 ,4-dioxane, 4-morpholine, 4-thiomorpholine, pyridine, pyridine-N- oxide or pyrimidine, or the following heterocycles:
• the term "9- or 10-membered heterobicycle” or “heterobicycle” either alone or in combination with another radical means a heterocycle as defined above fused to one or more other cycle, be it a heterocycle or any other cycle.
• heterobicycles include, but are not limited to, indole, benzimidazole, thiazolo[4,5-b]-pyridine, quinoline, or coumarin, or the following:
• Het defines a 4-, 5-, 6- or 7-membered heterocycle having 1 to 4 heteroatoms selected from O, N and S, which may be saturated, unsaturated or aromatic, or a 8-, 9-, 10- or 11 -membered heterobicycle having 1 to 5 heteroatoms wherever possible, selected from O, N and S, which-may be saturated, . unsaturated or aromatic, unless specified otherwise.
• HCy defines a saturated or unsaturated 4-, 5-, 6- or 7- membered monocyclic heterocycle having 1 to 3 heteroatoms selected from O, N and S, unless specified otherwise.
• Hetaryl defines an aromatic 5- or 6-membered monocyclic heterocycle having 1 or 2 heteroatoms selected from O, N and S, or a 9- or 10-membered aromatic heterobicycle having 1 to 4 heteroatoms selected from O, N, and S, unless specified otherwise.
• halo means a halogen atom and includes fluorine, chlorine, bromine and iodine.
• OH refers to a hydroxyl group. It is well known to one skilled in the art that hydroxyl groups may be substituted by functional group equivalents. Examples of such functional group equivalents that are contemplated by this invention include, but are not limited to, ethers, sulfhydryls, and primary, secondary or tertiary amines.
• the term "SH” refers to a sulfhydryl group. It is intended within the scope of the present invention that , whenever a "SH”.or "SR" group is present, it can also be substituted by any other appropriate oxidation state such as SOR, SO 2 R, or SO 3 R. i It is intended that the term "substituted” when applied in conjunction with a radical having more than one moiety such as C* ⁇ - 6 alkyl-aryl, or d- 6 alkyl-Het, such substitution applies to both moieties i.e. both the alkyl and aryl or Het moieties can be substituted with the defined substituents.
• COOH refers to a carboxylic acid group. It is well known to one skilled in the art that carboxylic acid groups may be substituted by functional group equivalents. Examples of such functional group equivalents that are contemplated by this invention include, but are not limited to, esters, amides, imides, boronic acids, tetrazoles, triazoles, N-acylsulfonyldiamides (RCONHSO 2 NR 2 ), and N- acylsulfonamides (RCONHSO 2 R).
• the term "functional group equivalent” is intended to mean an element or a substituted derivative thereof, that is replaceable by another element that has similar electronic, hybridization or bonding properties.
• metal catalyst is intended to mean a metal such as palladium (0) or palladium (2) for use in a cross-coupling reaction.
• palladium catalysts include, but are not limited to, Pd(Ph 3 ) 4 , Pd/C, Pd(OAc) 2 , PdCI 2 , and the like.
• Alternative metals that can catalyze cross-coupling reactions include, but are not limited to, complexes of Ni, Rh, Ru and Ir, like for example: Ni(acac) 2 , Ni(OAc) 2 , or NiCI 2 .
• detecttable label refers to any group that may be linked to the polymerase or to a compound of the present invention such that when the compound is associated with the polymerase target, such label allows recognition either directly or indirectly of the compound such that it can be detected, measured and quantified.
• labels are intended to include, but are not limited to, fluorescent labels, chemiluminescent labels, colorimetric labels, enzymatic markers, radioactive isotopes and affinity tags such as biotin. Such labels are attached to the compound or to the polymerase by well known methods.
• affinity tag means a ligand (that is linked to the polymerase or to a compound of the present invention) whose strong affinity for a receptor can be used to extract from a solution the entity to which the ligand is attached.
• ligands include biotin or a derivative thereof, a histidine polypeptide, a polyarginine, an amylose sugar moiety or a defined epitope recognizable by a specific antibody.
• affinity tags are attached to the compound or to the polymerase by well-known methods.
• photoreactive group means a group that is transformed, upon activation by light, from an inert group to a reactive species, such as a free radical.
• reactive species such as a free radical.
• examples of such groups include, but are not limited to, benzophenones, azides, and the like.
• salt thereof means any acid and/or base addition salt of a compound according to the invention; preferably a pharmaceutically acceptable salt thereof.
• pharmaceutically acceptable salt means a salt of a compound of formula (I) which is, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio,, generally water or oil-soluble or dispersible, and effective for their intended use.
• pharmaceutically-acceptable acid addition salts and pharmaceutically- acceptable base addition salts. Lists of suitable salts are found in, e.g., S.M. Birge et al., J. Pharm. Sci., 1977, 66, pp. 1-19, which is hereby incorporated by reference in its entirety.
• pharmaceutically-acceptable acid addition salt means those salts which retain the biological effectiveness and properties of the free bases and which are not biologically or otherwise undesirable, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfamic acid, nitric acid, phosphoric acid, and the like, and organic acids such as acetic acid, trifluoroacetic acid, adipic acid, ascorbic acid, aspartic acid, benzenesulfonic acid, benzoic acid, butyric acid, camphoric acid, camphorsulfonic acid, cinnamic acid, citric acid, digluconic acid, ethanesulfonic acid, glutamic acid, glycolic acid, glycerophosphoric acid, hemisulfic acid, hexanoic acid, formic acid, fumaric acid, 2-hydroxyethane- sulfonic acid (isethionic acid), lactic acid, hydroxymaleic acid, malic acid, mal
• pharmaceutically-acceptable base addition salt means those salts which retain the biological effectiveness and properties of the free acids and which are not biologically or otherwise undesirable, formed with inorganic bases such as ammonia or hydroxide, carbonate, or bicarbonate of ammonium or a metal cation such as sodium, potassium, lithium, calcium, magnesium, iron, zinc, copper, manganese, aluminum, and the like. Particularly preferred are the ammonium, potassium, sodium, calcium, and magnesium salts.
• Salts derived from pharmaceutically- acceptable organic nontoxic bases include salts of primary, secondary, and tertiary amines, quaternary amine compounds, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion-exchange resins, such as methylamine, dimethylamine, trimethylamine, ethylamine, diethylamine, triethylamine, isopropylamine, tripropylamine, tributylamine, ethanoiamine, diethanolamine, 2-dimethylaminoethanol, 2-diethylaminoethanol, dicyclohexylamine, lysine, arginine, histidine, caffeine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperazine, piperidine, N- ethylpiperidine, tetramethylammonium compounds, tetraethyl
• antiviral agent means an agent (compound or biological) that is effective to inhibit the formation and/or replication of a virus in a mammal. This includes agents that interfere with either host or viral mechanisms necessary for the formation and/or replication of a virus in a mammal.
• Antiviral agents include, for example, ribavirin, amantadine, VX-497 (merimepodib, Vertex Pharmaceuticals), VX- 498 (Vertex Pharmaceuticals), Levovirin, Viramidine, Ceplene (maxamine), XTL-001 and XTL-002 (XTL Biopharmaceuticals).
• other anti-HCV agent means those agents that are effective for diminishing or preventing the progression of hepatitis C related symptoms of disease.
• agents can be selected from: immunomodulatory agents, inhibitors of HCV NS3 protease, other inhibitors of HCV polymerase or inhibitors of another target in the HCV life cycle.
• immunomodulatory agent means those agents (compounds or biologicals) that are effective to enhance or potentiate the immune system response in a mammal.
• Immunomodulatory agents include, for example, class I interferons (such as ⁇ -, ⁇ -, ⁇ - and omega interferons, tau-interferons, consensus interferons and asialo- interferons), class II interferons (such as ⁇ -interferons) and pegylated interferons.
• inhibitor of HCV NS3 protease means an agent (compound or biological) that is effective to inhibit the function of HCV NS3 protease in a mammal.
• Inhibitors of HCV NS3 protease include, for example, those compounds described in WO 99/07733, WO 99/07734, WO 00/09558, WO 00/09543, WO 00/59929 or WO 02/060926, the Boehringer Ingelheim clinical candidate identified as BILN 2061 and the Vertex pre-development candidate identified as VX-950.
• compounds # 2, 3, 5, 6, 8, 10, 11 , 18, 19, 29, 30, 31 , 32, 33, 37, 38, 55, 59, 71 , 91 , 103, 104, 105, 112, 113, 114, 115, 116, 120, 122, 123, 124, 125, 126 and 127 disclosed in the table of pages 224-226 in WO 02/060926, can be used in combination with the compounds of the present invention .
• other inhibitor of HCV polymerase means an agent (compound or biological) that is effective to inhibit the function of HCV polymerase in a mammal, whereby this agent has a structure different from the compounds according to this invention and preferably binds to a site of the HCV polymerase different from the site targeted by the compounds according to this invention.
• Other inhibitors of HCV polymerase include non-nucleosides, for example, those compounds described in : WO 03/040112 (Rigel), WO 02/100846 A1 (Shire), WO 02/100851 A2 (Shire), WO 01/85172 .
• inhibitors of HCV polymerase also include nucleoside analogs, for example, those compounds described in: WO 01/90121 A2 (Idenix), WO 02/069903 A2 (Biocryst Pharmaceuticals Inc.), WO 02/057287 A2 (Merck/lsis) and WO 02/057425 A2 (Merck/lsis).
• inhibitor of another target in the HCV life cycle means an agent (compound or biological) that is effective to inhibit the formation and/or replication of HCV in a mammal other than by inhibiting the RNA dependent RNA polymerase of HCV. This includes agents that interfere with either host or HCV viral mechanisms necessary for the formation and/or replication of HCV in a mammal.
• Inhibitors of another target in the HCV life cycle include, for example, agents that inhibit a target selected from a HCV helicase, HCV NS2/3 protease and HCV IRES.
• Specific examples of inhibitors of another target in the HCV life cycle include ISIS- 14803 (ISIS Pharmaceuticals).
• HIV inhibitor means an agent (compound or biological) that is effective to inhibit the formation and/or replication of HIV in a mammal. This includes agents that interfere with either host or viral mechanisms necessary for the formation and/or replication of HIV in a mammal. HIV inhibitors include, for example, nucleosidic inhibitors, non-nucleosidic inhibitors, protease inhibitors, fusion inhibitors and integrase inhibitors.
• HAV inhibitor means an agent (compound or biological) that is effective to inhibit the formation and/or replication of HAV in a mammal. This includes agents that interfere with either host or viral mechanisms necessary for the formation and/or replication of HAV in a mammal.
• HAV inhibitors include Hepatitis A vaccines, for example, Havrix ® (GlaxoSmithKline), VAQTA ® (Merck) and Avaxim ® (Aventis Pasteur).
• HBV inhibitor means an agent (compound or biological) that is effective to inhibit the formation and/or replication of HBV in a mammal. This includes agents that interfere with either host or viral mechanisms necessary for the formation and/or replication of HBV in a mammal.
• HBV inhibitors include, for example, agents that inhibit HBV viral DNA polymerase or HBV vaccines.
• HBV inhibitors include Lamivudine (Epivir-HBV ® ), Adefovir Dipivoxil, Entecavir, FTC (Coviracil ® ), DAPD (DXG), L-FMAU (Clevudine ® ), AM365 (Amrad), Ldt (Telbivudine), monoval-LdC (Valtorcitabine), ACH-126,443 (L-Fd4C) (Achillion), MCC478 (Eli Lilly), Racivir (RCV), Fluoro-L and D nucleosides, Robustaflavone, ICN 2001-3 (ICN), Bam 205 (Novelos), XTL-001 (XTL), Imino-Sugars (Nonyl-DNJ) (Synergy), HepBzyme; and immunomodulator products such as: interferon alpha 2b,-' HE2000 (Hollis-Eden), Theradigm
• class I interferon means an interferon selected from a group of interferons that all bind to receptor type I. This includes both naturally and synthetically produced class I interferons. Examples of class I interferons include -, ⁇ -, omega interferons, tau-interferons, consensus interferons, asialo-interferons.
• class II interferon as used herein means an interferon selected from a group of interferons that all bind to receptor type II. Examples of class II interferons include ⁇ - interferons.
• ⁇ antiviral agents ribavirin and amantadine
• ⁇ immunomodulatory agents class I interferons, class II interferons and pegylated interferons;
• HCV NS3 protease inhibitors ⁇ HCV NS3 protease inhibitors; ⁇ other inhibitors of the HCV polymerase: nucleosidic and non-nucleosidic inhibitors;
• ⁇ inhibitor of another target in the HCV life cycle that inhibits a target selected from: HCV NS2/3 protease or internal ribosome entry site (IRES); ⁇ HIV inhibitors: nucleosidic inhibitors, non-nucleosidic inhibitors, protease inhibitors, fusion inhibitors and integrase inhibitors; or
• ⁇ HBV inhibitors agents that inhibit viral DNA polymerase or is an HBV vaccine.
• combination therapy is contemplated wherein a compound of formula (I), or a pharmaceutically acceptable salt thereof, is co-administered with at least one additional agent selected from: an antiviral agent, an immunomodulatory agent, an inhibitor of HCV NS3 protease, another inhibitor of HCV polymerase, an inhibitor of another target in the HCV life cycle, an HIV inhibitor, an HAV inhibitor and an
• HBV inhibitor examples of such agents are provided in the Definitions section above.
• additional agents may be combined with the compounds of this invention to create a single pharmaceutical dosage form. Alternatively these additional agents may be separately administered to the patient as part of a multiple dosage form, for example, using a kit. Such additional agents may be administered to the patient prior to, concurrently with, or following the administration of wherein a compound of formula (I), or a pharmaceutically acceptable salt thereof.
• treatment means the administration of a compound or composition according to the present invention to alleviate or eliminate symptoms of the hepatitis C disease and/or to reduce viral load in a patient.
• prevention means the administration of a compound or composition according to the present invention post-exposure of the individual to the virus but before the appearance of symptoms of the disease, and/or prior to the detection of the virus in the blood.
• Q 1 , Q 1c , Q 2 , Q 2a , Q 2b , Q 2c , W 1 , W 2 , Y°, Y 1 , Y 2 , Y 3 , X, Z, Sp, Het, HCy, Hetaryl, k 1t q, qa, and qb have the meanings as defined hereinbefore and hereinafter.
• groups, substituents and indices according to this invention are described.
• a or B is N and the other B or A is C, wherein — between two C-atoms represents a double bond and — between a C-atom and a N-atom represents a single bond,
• Sp is a spacer group selected from -(CR 51 R 52 ) k1 -, wherein k1 is 1 , 2 or 3;
• R 51 , R 52 are independently H, (d. 6 )alkyl, (C 3 . 7 )cycloalkyl or (d- ⁇ alkyl-
• R 51 and R 52 are covalently bonded together and to the carbon-atom to which they are attached to form a (C 3 . 6 )cycloalkyl group, said alkyl, cycloalkyls or alkyl-cycloalkyl being optionally substituted by halogen, hydroxy, (d- 6 )alkoxy, cyano, amino, -NH(d--ralkyl) and/or -N(d- 4 ⁇ alkyl) 2 ;
• Y° is O, S, NR 11 or CR 12 R 13 , wherein
• R 11 , R 12 , R 3 are each independently defined as R°;
• R 13 may also be COOR 0 or SO 2 R c ; wherein R c and each R° is optionally substituted with R 150 ;
• R 12 and R 13 are covalently bonded together and to the carbon-atom to which they are attached to form a 3, 4, 5, 6 or 7-membered saturated or 5, 6 or 7-membered unsaturated cyclic system whereby the 5, 6 or 7-membered saturated or unsaturated cyclic system may contain 1 to 3 heteroatoms selected from N, O or S; said cyclic systems being optionally substituted with
• L is d. 6 alkyl, (C 3 . 6 )cycloalkyl, C ⁇ . 6 alkyl-(C 3 -6)cycloalkyl, (C 2 . 6 )alkenyl, aryl,
• L may also be H
• L may also be OR c , wherein R c is optionally substituted with R 60 ;
• L may also be N(R 2 )R N1 , NR N3 -N(R N2 )R N1 , NR N3 -NR N2 -CO-R c , NR N4 -NR N3 -CO-N(R N2 )R N ⁇ NR N2 -SO 2 -R c , NR N2 -CO-R c , NR N3 -CO-N(R N2 )R N1 or N(R N1 )OR°; said R N1 , including any heterocycle or heterobicycle formed by R N1 , R N2 and/or R N3 , and R c and R° being optionally substituted with R 60 ;
• L may also be OR 6a or N(R 5a )R 6a , wherein R 5a is defined as R N2 ,
• R 6a is:
• R 7a and R 8a are each independently defined as R°, wherein said R° is optionally substituted with R 60 ;
• R 7a and R 8a are covalently bonded together to form a (C 3 . 7 )cycloalkyl or a 4, 5- or 6-membered heterocycle having from 1 to 3 heteroatom selected from O, N, and S; and when L is N(R Sa )R 6a , either of R 7a or R 8a may be covalently bonded to R 5a to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said cycloalkyl or heterocycle being optionally substituted by R 1 ⁇ 0 ; and
• Y 2 is O or S
• R 9a is defined as R°, wherein said R° is optionally substituted with R 60 ; or R 9a is covalently bonded to either of R 7a or R 8a to form a 5- or 6-membered heterocycle;
• Q 1 is aryl, Het, (d- 6 )alkyl-aryl, (d- 6 )alkyl-Het, (Ci-e alkyl-CONH-aryl or (d- 6 ) alkyl-CONH-Het, all of which being optionally substituted with R 60 ;
• Y 1 is O, S or NR 14 , wherein R 14 is H or (d-e) alkyl;
• Z is defined as a) OR 0 ; b) SO 2 R c ; c) N(R N2 )R N1 ; d) NR N3 -N(R N2 )R N1 ; e) NR N3 -NR N2 -CO-R c ; f) NR N4 -NR N3 -CO-N(R N2 )R N ; g) NR N2 -SO 2 -R c or h) NR N2 -CO-R c ; i) COOR 0 ; j) N(R N1 )OR°; wherein R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 , R N2 , and/or R N3 , being optionally substituted with R 60 ;
• R 7b , R 8b , Y 3 , R 9b , Q 2 are defined as R 7a , R 8a , Y 2 , R 9a , Q 1 , respectively;
• R 2 is selected from: halogen or R 21 , wherein R 21 is aryl or Het, said R 2i is optionally substituted with R 150 ;
• R 3 is selected from (C 1 - 6 )alkyl, (C 3 - 7 )cycloalkyl, (C 1 . 3 )alkyl-(C 3 . 7 )cycloalkyl,
• alkyl-HCy wherein HCy is a saturated or unsaturated 4 to 7-membered heterocyclic group with 1 to 3 heteroatoms selected from O, S and N; said alkyl, cycloalkyl, cycloalkenyl, bicycloalkyl, bicycloalkenyl, HCy and alkyl-HCy being optionally substituted with from 1 to 4 substituents selected from: a) halogen; b) (d- 6 )alkyl optionally substituted with:
• R 31 is H, (d-ealkyl), (C 3 . 7 )cycloalkyl or (d. 3 )alkyl-(C 3 - 7 )cycloalkyl; or
• each R 32 is independently H, (dialkyl, (C 3 . )cycloalkyl or (C ⁇ - 3 )alkyl-(C 3 - )cycloalkyl; or both R 32 are covalently bonded together and to the nitrogen to which they are attached to form a 5, 6 or 7-membered saturated heterocycle; c) OR 33 or SR 33 wherein R 33 is H, (C ⁇ - 6 )alkyl, (C 3 - 7 )cycloalkyl or (C ⁇ - 3 )alkyl-(C 3 - 7 )cycloalkyl; d) N(R 35 ) 2 wherein each R 35 is independently H, (C 1 .
• R 35 are covalently bonded together and to the nitrogen to which they are attached to form a 5, 6 or 7-membered saturated heterocycle;
• R 4a , R 4b , R 5 each are independently H or defined as R 150 ;
• R 150 b) OR 0 ; c) OC(O)R°; d) SR°, SO 2 R c , SO 2 N(R N2 )R N1 , SO 2 N(R N2 )C(O)R c or CONR N SO 2 R c ; e) N(R N2 )R N1 , N(R N2 )COOR c , or N(R N2 )SO 2 R c ; f) N(R N2 )COR c ; g) N(R N3 )CON(R N2 )R N1 ; h) N(R N3 )COCOR c , N(R N3 )COCOOR° or N(R N3 )COCON(R N2 )R N ; i) COR 0 ; j) COOR 0 ; k) CON(R N2 )R N1 ; I) aryl, Het, (C ⁇ alky ary
• R N1 is as defined or OH, O-C ⁇ -alkyl; i) COR 0 ; j) COOR°; k) tetrazole or CON(R N2 )R N1 ; wherein said R N1 , R c and/or R° are optionally substituted with R 60 as defined;
• R 160 is each defined as 1 , 2 or 3 substituents independently selected from: - 1 , 2 or 3 fluorine substituents; and - one of each substituent selected from tetrazole, chlorine, bromine, iodine,
• R° R c are independently defined as (C 1 . 6 )alkyl, (C 3 . 6 )cycloalkyl, (d- 4 )alkyl-
• R N1 is independently selected from H, (d- 6 )alkyl, (C 3 . 7 )cycloalkyl, (d- 4 .alkyl-
• R N2 , R N3 , R N4 are independently H, CH 3 , (C 2 . 6 alkyl), (C 3 . 6 )cycloalkyl, (d ⁇ alkyl-
• (C 3 . 6 )cycloalkyl wherein said alkyl, cycloalkyl or alkylcycloalkyl is optionally substituted with hydroxy, halogen, carboxy, C* ⁇ . 6 -alkoxycarbonyl, C* ⁇ - 6 -alkyl, C ⁇ e-alkoxy, amino, -NH(C 1 - 4 -alkyl) and/or -N(d- -alkyl) 2 ; and wherein said CH 3 is optionally substituted with halogen, carboxy or d- 6 -alkoxycarbonyl; and
• a) of a group N(R N2 )R N1 the substituents R N2 and R N1 ; or b) of a group NR N3 -N(R N2 )R N1 the substituents R N3 and R N1 , or R N2 and R N1 ; may be covalently bonded together to form a 4-, 5-, 6- or 7-membered saturated or unsaturated N-containing heterocycle or a 8-, 9-, 10- or 11- membered N-containing heterobicycle each may have additionally from 1 to 3 heteroatoms selected from O, N, and S; wherein Het is defined as a 4-, 5-, 6- or 7-membered heterocycle having 1 to 4 heteroatoms selected from O, N and S, or a 8-, 9-, 10- or 11 -membered heterobicycle having 1 to 5 heteroatoms selected from O, N and S;
• This invention comprises compounds of the formulas la and lb
• this invention further comprises compounds, of the following formulas:
• the groups M 1 and NI 4 are CR 4a and CR 4b , respectively.
• spacer group Sp is a group selected from -(CR 51 R S2 ) k , wherein k1 is 1 , 2 or 3; and R 51 , R 52 are independently H or (d. 3 )alkyl, in particular H or methyl; arid/or
• R 51 , R 52 are covalently bonded together and to the carbon-at ⁇ m to which they are > attached to form a cyclopropyl, cyclobutyl or cyclopentyl group.
• Sp is a spacer group selected from -CH 2 -, -CH(CH 3 )-, -C(CH 3 ) 2 -,
• Y° is O or S, most preferably O.
• Y° and L are covalently bonded to form a 5, 6, 7 or 8-membered mono- or a 8, 9, 10 or 11- membered bicyclic group which may contain 1 , 2 or 3 heteroatoms selected from N, O and S, wherein the mono- or bicyclic group is optionally substituted with R 60 .
• those compounds are preferred, wherein Y° and L are covalently bonded to form an unsaturated 5 or 6-membered monocyclic group which may contain 1 or 2 heteroatoms selected from N, O and S, wherein the monocyclic group is optionally substituted with R 60 .
• said monocyclic group is a monocyclic aromatic or heteroaromatic group.
• Preferred examples of such (hetero)aromatic groups are phenyl, pyridine and thiazole, being optionally substituted as described.
• Y° may also be NR 11 or CR 12 R 13 wherein R 11 , R 12 , R 3 are defined as hereinbefore.
• Preferred meanings of R 11 , R 2 , R 13 are independently H or C ⁇ - 6 alkyl; most preferably H or methyl.
• the group L has one of the following meanings: a) C*
• L may also be H; or c) if Y° is O, then L may also be OR c , wherein R c is optionally substituted with R 60 ,
• R 12 , R 13 , R 60 and R c are as defined hereinbefore.
• the group L has one of the following meanings:
• L is N(R N2 )R N1 , NR N3 -N(R N2 )R N1 , NR N3 -NR N2 -CO-R c , NR N4 -NR N3 -CO-N(R N2 )R N1 , NR N2 -SO 2 -R c or N(R N2 )OR°, said R N1 , including any heterocycle or heterobicycle formed by R N1 , R N2 and/or R N3 , and R c being optionally substituted with R 60 ; or
• L is N(R 5a )R 6a wherein R 5a is defined as R N2 and R 6a is:
• R 6a is:
• R 7a and R 8a are each independently defined as R°, wherein said R° is optionally substituted with R 80 ;
• R 7a and R 8a are covalently bonded together to form a second (C 3 . 7 )cycloalkyl or a 4, 5- or 6-membered heterocycle having from 1 to 3 heteroatom selected from O, N, and S; and either of R 7a or R 8a may be covalently bonded to R 5a to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said " cycloalkyl or heterocycle being optionally substituted by R 150 ; and
• Y 2 is O or S
• R 9a is defined as R°, wherein said R° is optionally substituted with R 60 ; or -
• R 9a is covalently bonded to either of R 7a or R 8a to form a 5- or 6-membered heterocycle
• Q 1 is aryl, Het, (d- 6 )alkyl-aryl, (d- 6 ) alkyl-Het, (d- ⁇ ) alkyl-CONH-aryl or (d. 6 ) alkyl-CONH-Het, all of which being optionally substituted with R 60 .
• the group Y 1 is defined as O, S or NR 14 , wherein R 14 is H or (C 1 . 6 )alkyl; most preferably Y 1 is O.
• the group Z is selected from the group of definitions: a) OR 0 ; c) N(R N2 )R N1 ; g) NR N2 -SO 2 -R c ; h) NR N3 -SO 2 -N(R N2 )R N1 ; or i) NR N2 -CO-R c ; wherein R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 and R N2 , being optionally substituted with R 60 ;
• R 7 , R 8b , Y 3 , R 9b , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively; and Q 2 is aryl, Het, (d-e) alkyl-aryl, (d- 6 )alkyl-Het, (d- 6 ) alkyl-CONH-aryl or (C 1 . 6 )alkyl- CONH-Het, all of which being optionally substituted with R 60 or Q 2 is R 160 or Q 2 is selected from the group consisting of O-C ⁇ - 4 -alkyl, S-C ⁇ -alkyl, C ⁇ . -alkyl, C 2 . 4 -alkenyl and C 2 - 4 -alkynyl, all of which being optionally substituted with R 160 ;.
• Y 1 is preferably O.
• Sp is a spacer group selected from -CH 2 -, -CH(CH 3 )-, -C(CH 3 ) 2 -,
• Y is O or S; most preferably O;
• L is N(R N2 )R N1 , NR N3 -N(R N2 )R N1 , NR N3 -NR N2 -CO-R c ,
• L is N(R 5a )R 6a wherein R 5a is defined as R N2 and R 6a is:
• R 6a is:
• Y 1 . is O or S; most preferably O;
• Z is defined as a) OR 0 ; c) N(R N2 )R N1 ; or g) NR N2 -SO 2 -R c ; wherein R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 and R N2 , being optionally substituted with R 60 ; or
• Z is N(R jS b b D* )% D R6 b b D , w.,h,e-..r.-e-.iinn o R ⁇ 0 b B : i tastess dceffiinnead a _-s o FTN"2 a __ndJ D R6b D ; is__.:
• R 6b is:
• R 7b , R 8b , Y 3 , R 9b , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively; and Q 2 is aryl, Het, (d-e) alkyl-aryl, (d- 6 ) alkyl-Het, (d-e) alkyl-CONH-aryl or (d-e) alkyl-CONH-Het, all of which being optionally substituted with R 60 or Q 2 is R 160 or Q 2 is selected from the group consisting of O-C ⁇ -4-alkyl, S-C-M-alkyl, C-M- alkyl, C ⁇ -alkenyl and C 2 -- * .-alkynyl, all of which being optionally substituted with R 160 ;.
• a first group of preferred compounds according to this invention is defined by formula 1.1a
• R N including any heterocycle formed by R N1 and R N2 , is optionally substituted with R 60 ;
• R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 and R N2 , being optionally substituted with R 60 ; or
• Z is N(R Sb )R 6 wherein R 5b is defined as R N2 and R 6b is:
• R bD is:
• R 7b , R 8b , Y 3 , R 9b , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively;
• Q 2 is aryl, Het, (d. 6 )alkyl-aryl, (d- 6 ) alkyl-Het, (d-e) alkyl-CONH-aryl or (d- 6 ) alkyl-CONH-Het, all of which being optionally substituted with R 60 or Q 2 is R 160 or Q 2 is selected from the group consisting of O-C ⁇ -alkyl, S-C- M -alkyl, C ⁇ - 4 - alkyl, C ⁇ -alkenyl and C ⁇ -alkynyl, all of which being optionally substituted with R 160 ;.
• a second group of preferred compounds according to this invention is defined by formula 1.1b
• R 5a is defined as R N2 ;
• R j7'a a , n R8a , ⁇ ⁇ 2, Q R9 a a , Q «1 1 , ⁇ WI ⁇ I1 1 are defined as hereinbefore;
• Z is defined as a) OR°; c) N(R N2 )R N1 ; or g) NR N2 -SO 2 -R c ; wherein R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 and R N2 , being optionally substituted with R 60 ; or
• R 7b , R 8b , Y 3 , R 9b , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively;
• Q 2 is aryl, Het, (d-e) alkyl-aryl, (d- 6 ) alkyl-Het, (d- 6 ) alkyl-CONH-aryl or (C.. 6 ) alkyl-CONH-Het, all of which being optionally substituted with
• R 60 or Q 2 is R 160 or Q 2 is selected from the group consisting of O-d- 4 -alkyl, S-C ⁇ - alkyl, C ⁇ - 4 -alkyl, C 2 ⁇ -alkenyl and C- M -alkynyl, all of which being optionally substituted with R 160 ;.
• a third group of preferred compounds according to this invention is defined by formula 1.1c
• R is optionally substituted with R ;
• R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 and R N2 , being optionally substituted with R 60 ; or
• R 5b is defined as R N2 and R 6 is:
• R bD is:
• R 7b , R 8b , Y 3 , R , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively;
• Q 2 is aryl, Het, (C «) alkyl-aryl, (Ci-e) alkyl-Het, (C ⁇ e) alkyl-CONH-aryl or (d- 6 ) alkyl-CONH-Het, all of which being optionally substituted with
• R 60 or Q 2 is R 160 or Q 2 is selected from the group consisting of alkyl, d- 4 -alkyl, C ⁇ -alkenyl and C 2 - 4 -alkynyl, all of which being . optionally substituted with R 160 ;.
• a fourth group of preferred compounds according to this invention is defined by formula l.1d
• R N1 is selected from OR c , NR N3 -N(R N2 )R N , NR N3 -NR N2 -CO-R c , NR N4 -NR N3 -CO-N(R N2 )R N1 or N(R N )OR°; said R N1 , including any heterocycle or heterobicycle formed by R N1 , R N2 and/or R N3 , and R c being optionally substituted with R 60 ;
• R° and R c are optionally substituted with R 60 ; and said R N1 , including any heterocycle or heterobicycle formed by R N1 and R N2 , being optionally substituted with R 60 ; or
• R , b 5b D is defined as R N N 2 ⁇ and R ⁇ 6 6 b D i is:
• R 6b is:
• R 7b , R 8b , Y 3 , R 9 , W 2 are defined as R 7a , R 8a , Y 2 , R 9a , W 1 respectively;
• Q 2 is aryl, Het, (d- 6 ) alkyl-aryl, (d-e) alkyl-Het, (d- 6 ) alkyl-CONH-aryl or (C ⁇ - 6 ) alkyl-CONH-H.et, all of which being optionally substituted with R 60 .
• Q 2 is R 160 or Q 2 is selected from the group consisting of O-d- 4 -alkyl, S-C**. 4 -alkyl, d- 4 - alkyl, C 2 . 4 -alkeny! and C ⁇ -alkynyl, all of which being optionally substituted with R 60 ;.
• L is more preferably
• R N2 , R N3 , R N4 are each independently H, methyl, (C 2 --t)alkyl, (C 3 . 6 )cycloalkyl or (C ⁇ .3)alkyl-(C 3 - 6 )cycloalkyl, all of which being optionally substituted with C ⁇ - 3 -alkyl, halogen, carboxy or (d- ⁇ alkoxycarbonyl; and/or wherein said alkyl, cycloalkyl or alkyl-cycloalkyi, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy, amino, -NH(d- 4 -alkyl), -N(C ⁇ - 4 -alkyl) 2 and/or - O-(d. 4 -alkyl);
• R N1 is H, methyl, (C ⁇ alkyl, (C 3 - 6 )cycloalkyl, (C 1 . 3 )alkyI-(C 3 . 6 )cycloalkyl, benzyl, (C 2 .
• the substituents R N and R N3 or R N1 and R N2 may be covalently bonded together to form a 5-, 6- or 7-membered saturated or unsaturated heterocycle which may have additionally 1 or 2 heteroatoms or a 8-, 9-, 10- or 11-membered saturated or unsaturated heterobicycle which may have additionally from 1 , 2 or 3 heteroatoms, whereby the heteroatoms are selected from O, N, and S; and
• Het is a 4-, 5-, 6- or 7-membered, preferably 5- or 6-membered, monocyclic group which contains 1 or 2 heteroatoms selected from N, O and S, wherein a benzene ring may be fused to the monocyclic group;
• phenyl group, heterocycle, heterobicycle or Het is optionally substituted by 1 to 4 substituents independently selected from:
• each substituent selected from: NO 2 , cyano, azido; and - 1 to 3 substituents selected from: (C ⁇ - 4 ,alkyl, hydroxy, O-(C ⁇ -4)alkyl, amino, -COOH,
• >N1 is methyl, (C 2 . 6 )alkyl, (C 3 . 7 )cycloalkyl, (C ⁇ - 3 .alkyl-(C 3 . 7 )cycloalkyl, benzyl, (C 2 -_*.)alkyl-phenyl, Het and (C* ⁇ - )alkyl-Het; wherein the methyl and alkyl groups are optionally substituted with C*t- 3 -alkyl, halogen, carboxy or (d- 4 ,alkoxycarbonyl, CONH 2 , CONH(C ⁇ - 4 -alkyl), CON(d- 4 -alkyl) 2 ; and/or wherein said alkyl, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy, amino, -NH(C 1 - 4 -alkyl), -N(d- 4 -alkyl) 2 and/or -O-(C ⁇
• Het is a saturated or unsaturated 4-, 5-, 6- or 7-membered, preferably 5- or 6-membered, monocyclic group which contains 1 or 2 heteroatoms selected from N, O and S, wherein, a benzene ring may be fused to the monocyclic group;
• phenyl group, heterocycle, heterobicycle or Het is optionally substituted by 1 to 4 substituents independently selected from: - 1 to 3 substituents selected from halogen; - one of each substituent selected from: NO 2 , cyano, azido; and
• R N2 very preferred meanings for R N2 are selected from H, methyl, ethyl, n-propyl, i-propyl, cyclopropyl and cyclopropylmethyl; in particular H and methyl; and
• R N1 is selected from methyl, ethyl, n-propyl, i-propyi, 1-methylpropyl, 2- methylpropyl, (C 4 . 7 )cycloalkyl, (C . 7 )cycloalkylmethyl-, (C - 7 )cycloalkylethyl-, (C . 7 )cycloalkenyl, (C . 7 )cycloalkenylmethyl-, (C . 7 )cycloalkenylethyl-, HCy-,
• Hetaryl is an aromatic 5 or 6-membered monocyclic group which contains 1 or 2 heteroatoms selected from N, O and S; to which a benzene ring may be fused; and
• HCy is a 4-, 5-, 6- or 7-membered saturated or mono-unsaturated heterocyclic group which contains 1 or 2 heteroatoms selected from N, O, S;
• each substituent selected from: chlorine bromine, NO 2 , cyano;
• substituents selected from: methyl, ethyl, n-propyl, i-propyl, cyclopropyl, cyclobutyl, cyclopentyl, hydroxy, C ⁇ . 3 -alkoxy, -COOH,
• the C-atom in ⁇ -position to the N-atom (of the group N(R N2 )R N1 ) is optionally ' substituted with methyl, CH 2 OH, CH 2 NH 2 , CH 2 NH(C 1 . 3 -alkyl), CH 2 N(d- 3 - alkyl) 2 , carboxy, (d-3)alkoxycarbonyl, CONH 2 , CONH(C 1 . 3 -alkyl), CON(C 1 . 3 - alkyl) 2 ; and/or, preferably or,
• any C-atom in ⁇ -position to the N-atom (of the group N(R N2 )R N1 ) is optionally substituted with hydroxy, C**. 3 -a!koxy, amino, -NH(C ⁇ . 3 -alkyl) or -N(d- 3 -alkyl) 2 .
• each R is independently H, methyl, ethyl, n-propyl, i-propyl or cyclopropyl; most preferably H or methyl.
• R N2 and R N1 are covalently bonded together to form a heterocycle selected from azetidine, pyrrolidine, piperidine, piperazine, morpholine, thiomorpholine, homopiperidine and homopiperazine;
• piperazine and homopiperazine may be N-substituted with C h alky!, (C 3 . 6 )cycloalkyl or C lJt alkyl-(C 3 - 6 )cycloalkyl;
• heterocycles are optionally monosubstituted by (C 3 . 6 )cycloalkyl, (C ⁇ . 3 )alkyl-(C 3 - 6 )cycloalkyl, HCy or C ⁇ alkyl-HCy , wherein HCy is selected from azetidine, pyrrolidine, piperidine, piperazine, morpholine, thiomorpholine, homopiperidine and homopiperazine; and
• heterocycles including an optional alkyl-, cycloalkyl- or alkylcycloalkyl-group and/or HCy or d. 3 alkyl-HCy group, are optionally substituted by 1 to 4 substituents independently selected from:
• substituents selected from: hydroxy, O-(d- 4 .alkyl, amino, -COOH, -COO(d- 4 )alkyl, CONH 2 , CONH(d- 4 - alkyl), CON(d- 4 -alkyl) 2 , -NH(d. 6 -alkyl), -N(d- 6 -alkyl) 2 , -(d- ⁇ alkyl-OH, -(d- 4 ,alkyl-COOH, -(d- 4 .alkyl-COO(d- 4 .alkyl,
• each R is independently H, methyl, ethyl, n-propyl, i-propyl or cyclopropyl; most preferably H or methyl.
• Y° is O and L is OR 6a , or wherein Y° is O or S and L is N(R 5a )R 6a , wherein R 5a is defined as R N2 , and
• R is defined according to the following subformula: wherein '
• R 7a is defined as H, COOH, CONH 2 , (C 1 - 6 )alkyl, (Cwjc cloalkyl, (C ⁇ Jalkyl- (C 3 .e)cycloalkyl, (C 2 . 6 )alkenyl, aryl, Het, (C M )alkyl-aryl, all of which are optionally substituted with R 60 ; and
• ,sa is H or (dialkyl; or
• R 7a and R 8a are covalently bonded together to form a (C 3 - 7 )cycloalkyl or a 4, 5- or 6- membered heterocycle having from 1 to 3 heteroatom selected from O, N, and S; and
• R 7a or R 8a may be covalently bonded to R 5a to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said cycloalkyl or heterocycle being optionally substituted by R 150 ;
• alkylene and alkenylene groups according to b), c) and d) may be substituted with (C*
• Q 1 is a group of the subformula Ilia
• Q 1a is aryl, Hetaryl, (d- 3 ) alkyl-aryl or (d- 3 )alkyl-Hetaryl;
• Q 1b is phenyl or Hetaryl;
• Q 1c is a bond, O-d- 4 -alkyl, S-d- 4 -alkyl, d- 4 -alkyl, C 2 . -alkenyl or C 24 - alkynyl;
• R 1q is selected from H, CN, COOR 161 , CON(R 162 ) 2 , SO 2 N(R 162 ) 2 , -N(R 162 ) 2 , OR 161 , SR 161 , -NHCOR 162 , -NH-CO-COOR 161 , -NH-CO-CON(R 162 ) 2 , NHSO 2 R c , CONHSO 2 R c , SO 2 NHCOR c , tetrazole, triazole and CONHSO 2 N(R 162 ) 2 ;
• q is 0 or 1 ;
• each aryl, phenyl, Hetaryl, alkyl, alkenyl and/or alkynyl-groups is optionally substituted with R 160 ;
• Hetaryl is an aromatic 5- or 6-membered heterocycle having 1 or 2 heteroatoms selected from O, N, and S, or a 8-, 9- or 10-membered aromatic heterobicycle having 1 to 4 heteroatoms selected from O, N, and S.
• R 6a is defined as:
• R 7a and R 8a are each independently defined as R°, wherein said R° is optionally substituted with R 60 ; or R 7a and R 8a are covalently bonded together to form a second (C 3 . 7 )cycloalkyl or a 4, 5- or 6-membered heterocycle having from 1 to 3 heteroatom selected from. O, N, and S; and when L is N(R 5a )R 6a , either of R 7a or R 8a may be covalently bonded to R 5a to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said cycloalkyl or heterocycle being optionally substituted by R so ; . and
• Y 2 is O or S
• R 9a is defined as R°, wherein said R° is optionally substituted with R 60 ; or R 9a is covalently bonded to either of R 7a or R 8a to form a 5- or 6-membered heterocycle;
• Q 1 is a group of the subformula Ilia
• Q 1a is aryl, Hetaryl, (d. 3 ) alkyl-aryl or (d. 3 )alkyl-Hetaryl;
• Q 1b is phenyl or Hetaryl
• Q 1c is a bond, O-C ⁇ -4-alkyl, S-C ⁇ - 4 -alkyl, C ⁇ -4-alkyl, C 2 --*,-alkenyl or C 24 - alkynyl;
• R 1q is selected from H, CN, COOR 161 , CON(R 162 ) 2 , SO 2 N(R 162 ) 2 , -N(R 16 ) 2 , OR 161 , SR 161 , -NHCOR 162 , -NH-CO-COOR 61 , -NH-CO-CON(R 162 ) 2 , NHSO 2 R c , CONHSO 2 R c , SOzNHCpR 0 , tetrazole, triazole and CONHSO 2 N(R 62 ) 2 ;
• q O or l ;
• each aryl, phenyl, Hetaryl, alkyl, alkenyl and/or alkynyl-groups is optionally substituted with R 160 ;
• Hetaryl is an aromatic 5- or 6-membered heterocycle having 1 or 2 heteroatoms selected from O, N, and S, or a 8-, 9- or 10-membered aromatic heterobicycle having 1 to.4 heteroatoms selected from O, N, and S.
• Z is defined as OR 0 , wherein R° is optionally substituted with R 60 .
• R° is H, (C 3 - 6 )cycloalkyl, d-salkyKC-j- ⁇ Jcycloal yl, (C 2 . 6 )alkenyl, (C ⁇ - 3 alkyl)phenyl, (C ⁇ . 3 )alkyl-pyridinyl, wherein said alkyl, alkyl-cycloalkyi, cycloalkyl, alkenyl, alkyl-phenyl or alkyl-pyridinyl is optionally substituted with
• R 162 are covalently bonded together and to the nitrogen to which they are attached to form a 5, 6 or 7-membered saturated heterocycle.
• a most preferred meaning of Z according to this embodiment is OH.
• Z is defined as N(R N2 )R N wherein R N1 , including any heterocycle or heterobicycle formed by R N and R N2 , is optionally substituted with R 60 .
• R N1 and R N2 in this embodiment are: R N2 is H, methyl, (d- ⁇ alkyi. dw cycloalkyl or (d- 3 )alkyl-(C 3 - 6 )cycloalkyl, all of which being optionally substituted with d- 3 -alkyl, halogen, carboxy or (d- )alkoxycarbonyl; and/or wherein said alkyl, cycloalkyl or alkyl-cycloalkyi, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy, amino, -NH(d_ 4 -alkyl), -N(C 1 - -alkyl) 2 and/or -O-(C ⁇ - 4 -alkyl); whereby R N2 is most preferably H; and
• R N is methyl, (C 2 -6)alkyl, (C 1 - 4 )alkyl-phenyl or (C ⁇ - 4 .alkyl-Het; wherein all of the methyl and alkyl groups are optionally substituted with C ⁇ . 3 -alkyl, halogen, carboxy or (C 1 - 4 )alkoxycarbonyl, CONH 2 , CONH(C 1 - 4 -alkyl), CON(C 1 - -alkyl) 2 ; and/or wherein said alkyl, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy, amino, -NH(d- 4 - alkyl), -N(C 1 . -alkyl) 2 and/or -O-(C ⁇ - 4 -alkyl); and
• Het is a 4-, 5-, 6- or 7-membered, preferably 5- or 6-membered, monocyclic group which contains 1 or 2 heteroatoms selected from N, O and S, wherein a benzene ring may be fused to the monocyclic group;
• phenyl group, heterocycle, heterobicycle or Het is optionally substituted by 1 to 4 substituents independently selected from:
• N-thiomorpholinyl N-piperazinyl, -(d- ⁇ alkyl-OH, -(C 1 - 4 )alkyl-O-(C 1 ⁇ )alkyl, -(d ⁇ alkyl-COOH, -(C 1 - 4 )aIkyl-COO(C 1 ⁇ )alkyl, -(C*,.
• R N1 and R N2 in this embodiment wherein Z is defined as N(R N2 )R N1 are:
• R N2 is H, methyl, ethyl, n-propyl, i-propyl, all of which being optionally substituted with methyl, fluorine, chlorine, carboxyl or methoxycarbonyl; and/or wherein said ethyl, n-propyl or i-propyl, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy, amino, - NH(CH 3 ), -N(CH 3 ) 2 and/or -O-(CH 3 );
• jN1 is methyl, ethyl, n-propyl, i-propyl, benzyl, phenylethyl, pyridinylmethyl or pyridinylethyl; wherein said methyl, ethyl, n-propyl, and i-propyl, groups are optionally substituted with fluorine, chlorine, methyl, ethyl, n-propyl, i-propyl,.
• phenyl and pyridinyl group is optionally substituted by 1 , 2 or 3 substituents independently selected from:
• substituents selected from: methyl, trifluoromethyl, ethyl, n-propyl, i-propyl, hydroxy, methoxy, ethoxy, -COOH, -COOCH 3 , CONH 2 , CONH(CH 3 ),
• R N2 is preferably H, methyl or ethyl, most preferably H
• R N1 is preferably benzyl or phenylethyl, both of which are optionally substituted with methyl, ethyl, n-propyl, i-propyl, fluorine, chlorine, carboxy, methoxycarbonyl, CONH 2 , CONH(CH 3 ), CON(CH 3 ) 2 ; and which at the phenyl group is optionally substituted with 1 , 2 or 3 substituents independently selected from:
• Z is defined as NR N2 -SO 2 -R G or NR N2 -CO-R c wherein R N2 and R c are preferably defined as follows:
• R N2 is H, (dialkyl, (C 3 - 6 )cycloalkyl or (d. 3 )alkyl-(C 3 - 6 )cycloalkyl; in particular H; and
• alkyl is (d-e)alkyl, (C 3 - 6 )cycIoalkyl, (C ⁇ - 3 )alkyl-(C 3 . 6 )cycloalkyl, (C 2 . 6 )alkenyl, phenyl, naphthyl, Het, (C* ⁇ - 3 )alkyl-phenyl, (d_ 3 )alkyt-naphthyl, (C
• R c is methyl, ethyl, n-propyl, i-propyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyi, pyrrolidine, piperidine, morpholine, thiomorpholine, piperazine, phenyl, naphthyl, benzyl, thiophene, furan, pyrrole, imidazole, pyrazole, oxazole, isoxazole, thiazole, pyridazine, pyrimidine, pyrazine, diazepine, azepine, quinoline, isoquinoline, benzofuran, benzothiophene, benzothiazole, purine, pteridine,
• R 60 substituents selected from R 60 , particularly OH, CN, halogen, nitro, (d. 3 )alkyl, O(d. 3 )alkyl, carboxyl, COO(d- 3 )alkyl, amino, NH(d- 3 )alkyl, N((C 1 - 3 )alkyl) 2 , NHCO(C*,. 3 )alkyl, wherein the alkyl groups may be substituted by halogen.
• R 5b is defined as R N2 and R 6b is:
• R 7b is defined as H, COOH, CONH 2 , (d- 6 )alkyl, (C 3 . 6 )cycloalkyl, (C ⁇ )alkyl- (C 3 - ⁇ )cycloalkyl, (C 2 - 6 )alkenyl, aryl, Het, (C ⁇ - 4 )alky ⁇ -aryl, (d- 4. alkyl-Het; all of which are optionally substituted with R 60 ; and
• ,8b is H or (dialkyl; or
• R 7b and R 8 are covalently bonded together to form a second (C 3 . 7 )cycloalkyl or a 4, 5- or 6-membered heterocycle having from 1 to 3 heteroatom selected from O, N, and S; and • when Z is N(R s )R 6b , either of R 7b or R 8b may be covalently bonded to R 5b to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said cycloalkyl or heterocycle being optionally substituted by R 150 ; and
• alkylene and alkenylene groups according to b), c) and d) may be substituted with (C*i- 3 ) alkyl;
• Q 2 is a group of the subformula Illb
• Q 2a is aryl, Hetaryl, (d. 3 ) alkyl-aryl or (d. 3 )alkyl-Hetaryl; . .
• Q 2b is phenyl or Hetaryl
• Q 2c is a bond, O-d- 4 -alkyl, S-C ⁇ -alkyl, C ⁇ - ⁇ -alkyl, C 2Jr alkenyl or
• R 170 is defined as H or as 1 , 2 or 3 substituents independently selected from:
• R is selected from H, CN, COOR 161 , CON(R 162 ) 2 , SO 2 N(R 16 ) 2 , -N(R 162 ) 2 , OR 161 , SR 161 , -NHCOR 162 ,'-NH-CO-COOR 161 , -NH-CO-CON(R 162 ) 2 , NHSO 2 R c , CONHSO 2 R c , SO 2 NHCOR c , tetrazole, triazole and CONHSO 2 N(R 162 ) 2 ; 5 qa is 0 or 1 ;
• qb is 0 or 1 ;
• each aryl, phenyl, Hetaryl, alkyl, alkenyl and/or alkynyl-groups is optionally substituted with R 160 ;
• Hetaryl is an aromatic 5- or 6-membered heterocycle having 1 or 2 heteroatoms selected from O, N, and S, or a 9- or 10-membered aromatic 15.
• heterobicycle having 1 to 4 heteroatoms selected from O, N, and S.
• index qa is 1.
• R 5b is defined as R N2 and R 6b i.
• R 7b and R 8b are each independently defined as R°, wherein said R° is optionally 25 substituted with R 60 ; or
• R 7b and R 8b are covalently bonded together to form a (C 3 . 7 )cycloalkyl or a 4, 5- or 6- membered heterocycle having from 1 to 3 heteroatom selected from O, N, and S; or when Z is N(R 5 )R 6b , either of R 7b or R 8b may be covalently bonded to R 5b 30 to form a nitrogen-containing 5-or 6-membered heterocycle, wherein said cycloalkyl or heterocycle being optionally substituted by R 150 ; and Y 3 is O or S;
• R 9 is defined as R°, wherein said R° is optionally substituted with R 60 ; or
• R 9b is covalently bonded to either of R 7b or R 8b to form a 5- or 6-membered heterocycle
• Q 2 is a group of the subformula 1Mb
• Q 2a is aryl, Hetaryl, (C 1 - 3 ) alkyl-aryl or (C 1 . 3 )alkyl-Hetaryl;
• Q 2b is a phenyl or Hetaryl;
• Q 2c is a bond, O-C ⁇ -alkyl, S-d- 4 -alkyl, d. 4 -alkyl, C ⁇ -alkenyl or C ⁇ -alkynyl, wherein said O-C ⁇ - -alkyl, S-d- 4 -alkyl, d. 4 -alkyl, C 2-4 -alkenyl or C ⁇ -alkynyl are optionally substituted with R 170 wherein R 170 is defined as H or as 1 , 2 or 3 substituents independently selected from:
• R 2 is selected from H, CN, COOR 161 , CON(R 162 ) 2 , SO 2 N(R 162 ) 2 , -N(R 162 ) 2 ,
• qa is 0 or 1 ;
• qb is 0 or 1 ; wherein each aryl, phenyl, Hetaryl, alkyl, alkenyl and/or alkynyl-groups is optionally substituted with R 160 ; and
• Hetaryl is an aromatic 5- or 6-membered heterocycle having 1 or 2 heteroatoms selected from O, N, and S, or a 9- or 10-membered aromatic heterobicycle having 1 to 4 heteroatoms selected from O, N, and S.
• index qa is 1.
• L is OR 6a or N(R N2 )R 6a wherein R 6a is:
• W 1 and W 2 or both W 1 and W 2 represent a single bond.
• R 7a and R 7b or both R 7a and R 7b are H, COOH, CONH 2 , CF 3 , (dialkyl, (C 3 . 7 )cycloalkyl, (C 1 . 3 )alkyl-(C 3 . 7 )cycloalkyl, Hetaryl or (d- 3 )alkyl- Hetaryl, wherein the alkyl, cycloalkyl groups and Hetaryl groups are optionally subsituted with R 160 .
• R 8a and R 8b or both R 8 8 a a a planted formuland J D R8 8 b B are H and CH 3
• R 7a and R 8a and/ or R 7b and R 8b are covalently bonded together to form a second (C 3 . 7 )cycloalkyl or a 4, 5- or 6-membered heterocycle having from 1 to 2 heteroatom selected from O, N, and S, wherein said cycloalkyl or heterocycle being optionally substituted with R 160 , preferably with 1 to 3 substituents selected from hydroxy, (d- 3 )alkyl, CO(C . 3 )alkyl and SO 2 (C ⁇ . 3 )alkyl.
• R 7a and R 7b is each independently preferably selected from COOH, CONH 2 , methyl, ethyl, n-propyl, i- propyl, 2-methylpropyl, hydroxy-m ethyl, 1-hydroxy-ethyl, amino-methyl, 1 -amino- . ethyl, 2-hydroxy-ethyl, 2-methylthio-ethyl, 2-amino-ethyl, 2-(dimethylamino)-ethyl and thiazolyl, wherein the thiazolyl group is optionally substituted with R 160 ; or
• R 7 and R 8b are covalently bonded together to form a cyclic group preferably selected from:
• the groups CR' a R Ba and CR 7'b D D R8 B b D are independently selected from
• R 9a and/or R 9b is preferably H, (d- 3 alkyl), (C 3 - 6 )cycloalkyi or
• Q and Q ⁇ 2a are independently selected from
• R L is H, (C ⁇ alkyl) or (C ⁇ - 4 )alkoxy
• R Q is H or CH 3 , (C 2 - 6 alkyl), -CH 2 -(C 2 . 6 alkenyl), -CH 2 -(C 2 . 6 alkynyl), (C 3 . 6 )cycloalkyl, (C ⁇ --t)alkyl-(C 3 - 6 )cycloalkyl; all of which being optionally substituted with d-e- alkyl, halogen, carboxy or C ⁇ - 6 -alkoxycarbonyl; and/or wherein said alkyl, cycloalkyl or alkylcycloalkyl, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy, C* ⁇ - 6 -aikoxy, amino, -NH(d- 4 -a!kyl) and/or -N(d_ -alkyl) 2 ;
• Q 1 and/or Q 2b are selected from the group consisting of phenyl, furan, thiophene, oxazole, thiazole, pyridine, pyrimidine, pyrrazole, imidazole and pyrazine.
• Q ⁇ 1b a sexual calendarn,d, ⁇ Q2b are independently selected from the group consisting of
• R 1q and R 2q are preferably selected from H, CN, COOR 161 , CON(R 162 ) 2 , SO 2 N(R 16 ) 2 , -N(R 162 ) 2 , OR 161 ,-NHCOR 162 , -NH-CO-COOR 161 , -NH-CO-CON(R 162 ) 2 , NHSO 2 R c , CONHSO 2 R c , SO 2 NHCOR c , tetrazole, triazole and CONHSO 2 N(R 162 ) 2 ; most preferably selected from COOR 161 , CON(R 162 ) 2 and SO 2 N(R 162 ) 2 ; wherein R 161 and R 162 are as defined, but most preferably H and/or methyl.
• Q and Q 2 are independently selected from:
• cyclic groups are optionally substituted with R 160 ; most preferably 1 or 2 substituents selected from fluorine, chlorine, bromine, OH, methoxy, ethoxy, amino, NH(CH 3 ), methyl, ethyl, i-propyl and n-propyl;
• R 170 is each independently defined as hereinbefore; preferably R 170 is defined as H, F, -CH 3 , -CH 2 CH 3 , -CF 3 , or cyclopropyl ; most preferably H, F, -CH 3 , or -CH 2 CH 3 ; and
• R° is each independently defined as hereinbefore; preferably R Q is defined as H, (d. 6 alkyl), (C 3 - 6 )cycloalkyl or (C 1 - 4 )alkyl-(C 3 . 6 )cycloalkyl; most preferably H or methyl.
• Q 1 and Q 2 are independently selected from:
• cyclic groups are optionally substituted with R 160 ; most preferably 1 or 2 substituents selected from fluorine, chlorine, bromine, OH, methoxy, ethoxy, amino, NH(CH 3 ), methyl, ethyl, i-propyl and n-propyl;
• R 170 is each independently defined as hereinbefore; preferably R 170 is defined as H, F, -CH 3 , -CH 2 CH 3 , -CF 3 , or cyclopropyl ; most preferably H, F, -CH 3 , or -CH 2 CH 3 ; and
• R Q is each independently defined as hereinbefore; preferably R Q is defined as H, (C ⁇ - 6 alkyl), (C 3 - 6 )cycloalkyl or (C 1 - )alkyl-(C 3 - 6 )cycloalkyl; most preferably H or methyl.
• Q 1a or Q 2a is a phenylene or Hetaryl group
• preferred substituents of this group are selected from (C ⁇ _ 3 )alkyl and (d. 3 )alkoxy, especially from methyl, ethyl, methoxy, ethoxy.
• Q 1 and Q 2 which are substituted are for example:
• R 170 is each independently defined as hereinbefore; preferably R 170 is defined as H, F, -CH 3 , -CH 2 CH 3 , -CF 3 , or cyclopropyl ; most preferably H, F, -CH 3 , or -CH 2 CH 3 ;.
• N(R 5a )R 6a and N(R 5b )R 6b are described for those cases wherein either L or Z, or both L and Z are defined as follows:
• examples of very preferred groups L and Z, in case qa is 1 are independently selected from the group consisting of:
• cyclic groups are optionally substituted with R ; most preferably 1 or 2 substituents selected from fluorine, chlorine, bromine, OH, methoxy, ethoxy, amino, NH(CH 3 ), methyl, ethyl, i-propyl and n-propyl;
• R 170 is each independently defined as hereinbefore; preferably R 170 is defined as H, F, -CH 3 , -CH 2 CH 3 , -CF 3 , or cyclopropyl ; most preferably H, F, -CH 3 , or -CH 2 CH 3 ; and
• R Q is each independently defined as hereinbefore; preferably R Q is defined as H, (d- 6 alkyl), (C . 6 )cycloalkyl or (C 1 - )alkyl-(C 3 - 6 )cycloalkyl; most preferably H or methyl.
• R Q is each independently defined as hereinbefore; preferably R Q is defined as H, (d- 6 alkyl), (C . 6 )cycloalkyl or (C 1 - )alkyl-(C 3 - 6 )cycloalkyl; most preferably H or methyl.
• preferred groups Z in case qa is 0, are independently selected from the group consisting of:
• N(R 5a )R 6a and N(R 5b )R 6b are described for those cases wherein either L orZ, or both.L and Z are defined as follows:
• L is N(R 5a )R ba wherein R 6a is:
• Z is N(R 5b )R 6b wherein R 6b is:
• L and Z are more preferably independently selected from the group consisting of:
• cyclic groups are optionally substituted with R 160 ; most preferably 1 or 2 substituents selected from fluorine, chlorine, bromine, OH, methoxy, ethoxy, amino, NH(CH 3 ), methyl, ethyl, i-propyl and n-propyl;
• R 170 is each independently defined as hereinbefore; preferably R 170 is defined as H, F, -CH 3 , -CH 2 CH 3 , -CF 3 , or cyclopropyl ; most preferably H, F, -CH 3 , or -CH 2 CH 3 ; and
• R Q is each independently defined as hereinbefore; preferably R Q is defined as H, (C* ⁇ - 6 alkyl), (C 3 - 6 )cycloalkyl or (C 1 - )alkyl-(C 3 . 6 )cycloalkyl; most preferably H or methyl.
• R 2 is R 21 , wherein R 21 is a phenyl or Het selected from the group of formulas
• R 2 as defined above is substituted, it is preferably substituted with 1 , 2 or 3 substituents selected from: - 1 to 3 substituents selected from halogen;
• R 2 is selected from:
• R 3 is preferably selected from (C 3 - 7 )cycloalkyl, (C 5 - 7 )cycloalkenyl, (C 6 . ⁇ o)bicycloalkyl, (C 6 . ⁇ o)bicycloalkenyl, or HCy wherein said groups are unsubstituted or mono- or disubstituted by halogen, hydroxy, dialkyl and/or O-d ⁇ alkyl, wherein the alkyl groups may be fluorinated.
• R 3 is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl,
• R 3 is cyclopentyl, or cyclohexyl.
• R a , R 4 , R 5 each are independently H, hydroxy, halogen, cyano, nitro, carboxyl, (C-uJalkyl, CF 3 , (d ⁇ )alkoxy, -O-(C 3 . 7 )cycloalkyl, -O-(C 1 . 3 )alkyl- (C 3 . 7 )cycloalkyI, -O-aryl, -O-(C*,.
• R 4a , R 4b , R 5 each are independently H, hydroxy, halogen, cyano, nitro, methyl, CF 3 . methoxy, carboxy, amino, -NMe 2 , -CONH 2 , -NHCONH 2 , -CO-NHMe, -NHCONHMe, -CO-NMe 2 or -NHCONMe 2 ; in particular H, methyl or methoxy.
• R 4a is H or methyl.
• Very most preferably at least two of the substituents selected from R 4a , R 4 , R 5' are H.
• the substituents R 60 are preferably each defined as 1 to 4 substituents independently selected from: - 1 to 3 substituents selected from halogen;
• Het is selected from furan, tetrahydrofuran, thiophene, tetrahydrothiophene, tetrahydropyran, pyridinyl, azetidine, pyrrolidine, piperidine, piperazine, morpholine, thiomorpholine, homopiperidine and homopiperazine;
• R N1 , R c and/or R° are optionally substituted with R 1so as defined.
• R 150 is preferably defined as 1 to 4 substituents independently selected from: - 1 to 3 fluorine-substituents; - one of each substituent selected from: chlorine, bromine, iodine, NO 2 , cyano, azido; and
• R 160 is preferably defined as 1 , 2 or 3 substituents independently selected from:
• each substituent selected from chlorine, bromine, iodine, CN, nitro, methyl, trifluoromethyl, ethyl, n-propyl, i-propyl, COOH, COOCH 3 , OH, OCH 3 , OCF 3 , NH 2 , NHCH 3 , N(CH 3 ) 2 , SO 2 NH 2 , NHCOCH 3 , SO 2 NHCOCH 3 , CONH 2 , CONHCH 3 and
• R°, R c are independently selected from (Chalky!, (C 3 - 6 )cycloaikyl, 20 (C ⁇ - 3 )alkyi-(C 3 . 6 )cycloalky), phenyl, benzyl, Het, (d- 3 )aIkyl-Het; all of which are optionally substituted as defined; and R° may also be H.
• R N1 is preferably selected from H, (dialkyl, (C 3 . 6 )cycloalkyl, (C**. 3 )alkyl-
• R N2 , R N3 , R N4 are independently selected from H, methyl, ethyl, n-propyl, i-propyl, cyclopropyl, cyclopropylmethyl; all of which being optionally substituted with methyl, fluorine, carboxy or methoxycarbonyl; and/or wherein said ethyl, n- propyl or i-propyl, but preferably not the C-atom thereof directly bonded to the N-atom, is optionally substituted with hydroxy* methoxy, amino, -NH(CH 3 )
• R N2 and R N1 may be covalently bonded together to form a 5-, 6- or 7-membered saturated heterocycle which may have additionally one heteroatom selected from O, N, and S, wherein said heterocycle is optionally substituted as defined.
• Preferred compounds according to this invention are listed in the tables. Particularly compounds of these tables are preferred which show an IC 50 value of below 200 nM, as for example those compounds included in the claims 51 , 52, 53, 54 and 55.
• RNA dependent RNA polymerase of HCV The ability of the compounds of formula (I) to inhibit RNA synthesis by the RNA dependent RNA polymerase of HCV can be demonstrated by any assay capable of measuring RNA dependent RNA polymerase activity.
• a suitable assay is described in the examples.
• the compounds of the invention act by specific inhibition of HCV polymerase, the compounds may be tested for inhibitory activity in a DNA dependent RNA polymerase assay.
• a compound of formula (I), or one of its therapeutically acceptable salts When a compound of formula (I), or one of its therapeutically acceptable salts, is employed as an antiviral agent, it is administered orally, topically or systemically to mammals, e.g. humans, cattle, pigs, dogs, cats, rabbits or mice, in a vehicle comprising one or more pharmaceutically acceptable carriers, the proportion of which is determined by the solubility and chemical nature of the compound, chosen route of administration and standard biological practice.
• the compound or a therapeutically acceptable salt thereof can be formulated in unit dosage forms such as capsules or tablets each containing a predetermined amount of the active ingredient, ranging from about 25 to 500 mg, in a pharmaceutically acceptable carrier.
• the compound can be formulated in pharmaceutically accepted vehicles containing 0.1 to 5 percent, preferably 0.5 to 5 percent, of the active agent.
• Such formulations can be in the form of a solution, cream or lotion.
• the compound of formula (I) is administered by either intravenous, subcutaneous or intramuscular injection, in compositions with pharmaceutically acceptable vehicles or carriers.
• pharmaceutically acceptable vehicles or carriers for administration by injection, it is preferred to use the compounds in solution in a sterile aqueous vehicle which may also contain other solutes such as buffers or preservatives as well as sufficient quantities of pharmaceutically acceptable salts or of glucose to make the solution isotonic.
• Suitable vehicles or carriers for the above noted formulations are described in pharmaceutical texts, e.g. in "Remington's The Science and Practice of Pharmacy", 19th ed., Mack Publishing Company, Easton, Penn., 1995, or in “Pharmaceutical Dosage Forms And Drugs Delivery Systems", 6th ed., H.C. Ansel et al., Eds., Williams & Wilkins, Baltimore, Maryland, 1995.
• the dosage of the compound will vary with the form of administration and the particular active agent chosen. Furthermore, it will vary with the particular host under treatment. Generally, treatment is initiated with small increments until the optimum effect under the circumstance is reached. In general, the compound of formula I is most desirably administered at a concentration level that will generally afford antivirally effective results without causing any harmful or deleterious side effects.
• the compound or a therapeutically acceptable salt is administered in the range of 10 to 200 mg per kilogram of body weight per day, with a preferred range of 25 to 150 mg per kilogram.
• the compound of formula (I) is administered at a dosage of 10 mg to 150 mg per kilogram of body weight per day, although the aforementioned variations will occur.
• a dosage level that is in the range of from about 10 mg to 100 mg per kilogram of body weight per day is most desirably employed in order to achieve effective results.
• compositions of this invention comprise a combination of a compound of formula I and one or more additional therapeutic or prophylactic agent
• both the compound and the additional agent should be present at dosage levels of between about 10 to 100%, and more preferably between about 10 and 80% of the dosage normally administered in a monotherapy regimen.
• these compounds or their pharmaceutically acceptable salts are formulated together with a pharmaceutically acceptable carrier, the resulting composition may be administered in vivo to mammals, such as man, to inhibit HCV polymerase or to treat or prevent HCV virus infection.
• Such treatment may also be achieved using the compounds of this invention in combination with agents which include, but are not limited to: immunomodulatory agents, such as ⁇ -, ⁇ -, or ⁇ -interferons; other antiviral agents such as ribavirin, amantadine; other inhibitors of HCV NS5B polymerase; inhibitors of other targets in the HCV life cycle, which include, but are not limited to, helicase, NS2/3 protease, NS3 protease, or internal ribosome entry site (IRES); or combinations thereof.
• immunomodulatory agents such as ⁇ -, ⁇ -, or ⁇ -interferons
• other antiviral agents such as ribavirin, amantadine
• other inhibitors of HCV NS5B polymerase inhibitors of other targets in the HCV life cycle, which include, but are not limited to, helicase, NS2/3 protease, NS3 protease, or internal ribosome entry site (IRES); or
• Indole derivatives or analogs according to the present invention can be prepared from known monocyclic aromatic compounds by adapting known literature sequences such as those described by J.W. Ellingboe et al. (Tet. Lett. 1997, 38, 7963) and S. Cacchi et al. (Tet. Lett. 1992, 33, 3915).
• Scheme 1 shown below wherein R 1 , R 2 , Sp, Y and L are as described herein, illustrate how these procedures can be adapted to the synthesis of compounds of formula I of this invention.
• a palladium metal complex such as PdCI 2 (PPh 3 ) 2 , Pd 2 dba 3 , Pd(PPh 3 ) 4 and the like), a base (EtsN, DIEA and the like or an inorganic basic salt including metal carbonates, fluorides and phosphates), and optionally in the presence of an additional phosphine ligand (triaryl or heteroarylphosphine, dppe, dppf, dppp and the like).
• Suitable solvents for this reaction include DMF, dioxane, THF, DME, toluene, MeCN, DMA and the like at temperatures ranging from 20 °C to 170 °C, or alternatively without solvent by heating the components together.
• the cross-coupling reaction can be carried out on a suitably protected form of 3-amino-4-iodobenzoate and the amino group can be trifluoroacetylated in the subsequent step as described by J.W. Ellingboe et al. (Tet. Lett. 1997, 38, 7963). Reaction of the above diarylalkynes l(iii) with an enol triflate or equivalent under cross-coupling conditions similar to those described above gives after hydrogenation of the double bond, indole derivatives l(iv).
• Enol triflates are known and can be prepared from the corresponding ketones by following known literature methods (for example, cyclohexene triflate can be prepared from cyclohexanone, triflic anhydride and a hindered organic base such as 2,6-di-fet -butyl-4-methylpyridine).
• the hydrogenation of the double bond originally present in R 3 can be carried out with hydrogen gas or a hydrogen donor (ammonium formate, formic acid and the like) in the presence of a metal catalyst (preferably Pd) in a suitable solvent (lower alkyl alcohols, THF etc.).
• indole derivative l(iv) is then alkylated on nitrogen with an appropriate spacer (Sp) and further elaborated if necessary to give ⁇ /-alkylated indole carboxylates where Y, Sp and L are as defined herein.
• the resulting carboxyindole derivative is converted to compounds of formula 1 by coupling with the appropriate Z group.
• Condensation of the 6-indolecarboxylic acid with amines or alcohols can be accomplished using standard amide bond forming reagents such as TBTU, HATU, BOP, BroP, EDAC, DCC, isobutyl chloroformate and the like, or by - activation of the carboxyl group by conversion to the corresponding acid chloride prior to condensation with an amine. Any remaining protecting group is removed following this step to give compounds of formula 1.1.
• compounds of formula 1.1 can be prepared by elaboration from a preexisting indole core by following adaptations of literature procedures as described, for example, by P. Gharagozloo et al. (Tetrahedron 1996, 52, 10185) or K. Freter (J. Org. Chem. 1975, 40, 2525). Such a methodology is illustrated in Scheme 2: SCHEME 2
• Suitable conditions to affect this condensation include strong bases such as alkali metal hydroxides, alkoxides and hydrides in solvents such as lower alkyl alcohols (MeOH, EtOH, terfBuOH etc.), THF, dioxane, DMF, DMSO, DMA and the like at reaction temperature ranging from -20 °C to 120 °C.
• solvents such as lower alkyl alcohols (MeOH, EtOH, terfBuOH etc.), THF, dioxane, DMF, DMSO, DMA and the like at reaction temperature ranging from -20 °C to 120 °C.
• the condensation can be carried out under acid conditions using organic or mineral acids or both.
• Appropriate conditions include mixtures of AcOH and aqueous phosphoric acid at temperatures ranging from 15°C to 120 °C.
• the carboxylic acid group is then protected in the form of an ester (usually lower alkyl) using known methods.
• Halogenation (usually bromination, but also iodination) of the 2-position of the indole 2(iii) gives 2(iv).
• Suitable halogenating agents include, for example, elemental bromine, ⁇ /-bromosuccinimide, pyridine tribromide, dibromohydantoin and the corresponding iodo derivatives.
• Suitable solvents for this reaction are inert to reactive halogenating agents and include for example hydrocarbons, chlorinated hydrocarbons (DCM, CCI 4 , CHCI 3 ), ethers (THF, DME, dioxane), acetic acid, ethyl acetate, IPA, and mixtures of these solvents. Reaction temperature ranges from -40 °C to 100 °C. A method of choice to carry out the bromination of indoles as shown in Scheme 2 was described by L. Chu (Tet. Lett. 1997, 38, 3871).
• the 2-bromoindole derivatives 2(iv) can be converted to fully substituted key intermediates l(v) by different sequences: (1) Trans-metallation of the 2- bromoindole to tin, boron, zinc species and the like, followed by cross-coupling reaction with aryl or heteroaryl halides under transition metal catalysis as described in scheme 1 gives indole derivative 2(vii) which can then be elaborated on nitrogen as described in scheme 1 to give key intermediate 1(v).
• the indoleic NH is optionally protected with known protecting groups such as BOC, MOM, SEM, SO 2 Ph and the like. The protecting group is removed at a later stage of the sequence, prior to linker attachment.
• the conversion of 2-bromoindole derivatives 2(iv) to the corresponding organotin species 2(vi) is carried out via initial low- temperature (usually -78 ° to -30 °C) halogen-metal exchange using an alkyllithium reagent (e.g. nBuLi or ferf-BuLi) or using lithium metal.
• an alkyllithium reagent e.g. nBuLi or ferf-BuLi
• the transient 2-lithioindole species is then trapped with a trialkyltin halide (e.g. nBu 3 SnCI or Me 3 SnCI) or a borate ester (e.g. trimethyl or triisopropyl borates).
• the lithioindole intermediate can be trapped with zinc chloride to form the corresponding organozincate which can also undergo transition metal-catalyzed cross-coupling with aromatic and heteroaromatic halides or triflates as described, for example, by M. Rowley (J. Med. Chem. 2001 , 44, 1603).
• species such as 2(vi) where the indoleic NH is masked with a protecting group can be generated directly from 2(iii) by ester formation followed by indole NH protection and abstraction of the 2-H proton with strong base (e.g. alkyllithiums, alkalimetal amides) followed by trans- metallation.
• 2-bromoindole 2(iv) can be cross-coupled directly to aryl and heteroaryl stannanes or boronic acid derivatives to give 2(vii) directly.
• Boron or tin organometallic species are from commercial sources or can be prepared by standard literature procedures.
• 2-bromoindole 2( ⁇ v) is first elaborated on nitrogen to give 2(v) which is then cross-coupled to R 2 to give the same intermediate 1 (v) as described above.
• Cross-coupling with organoboron reagents can be carried out by any variations of the Suzuki cross-coupling reaction reported in the literature.
• a transition metal catalyst usually Pd°
• triaryl or triheteroarylphosphine ligands an additive such as an inorganic chloride (e.g. LiCI)
• a base usually an aqueous inorganic base such as sodium or potassium carbonate or phosphate.
• EtOH alcoholic solvent
• DME toluene
• THF toluene
• Cross-coupling with tin reagents can be carried out by any variations of the Stille cross-coupling reaction reported in the literature.
• a transition metal catalyst usually Pd°
• triaryl or triheteroaryl phosphine ligands an additive such as an inorganic chloride (e.g. LiCI) or iodide (e.g. Cul).
• Suitable solvents for this reaction include toluene, DMF, THF, DME and the like at temperatures ranging from 25 °C to 140 °C.
• Intermediate l(v) is then converted to compounds of formula 1.1 as described for Scheme 1.
• Reaction conditions to alkylate the nitrogen of an indole derivative are well known to those skilled in the art and include the use of strong bases such as alkali metal hydrides, hydroxides, carbonates, amides, alkoxides and alkylmetals, in the appropriate solvent (such as THF, dioxane, DME, DMF, MeCN, DMSO, alcohols and the like) at temperatures ranging from -78 °C to 140 °C.
• An electrophilic form of Sp is used for the alkylation of the indole anion.
• electrophilic species include iodides, bromides, chlorides and sulfonate esters (mesylate, tosylate, brosylate or triflate).
• BroP Bromo tris(dimethylamino)phosphonium hexafluorophosphate Bu: butyl
• DIEA dusopropylethylamine
• DME dimethoxyethane
• DMF N./V-dimethylformamide
• DMSO dimethylsulfoxide
• dppe 1 ,2-bis(diphenylphosphino)ethane
• dppf 1 ,1'-bis(diphenylphosphino)ferrocene
• dppp 1 ,2-bis(diphenylphosphino)propane
• DTT dithiothreitol
• HATU O-(7-azabenzotriazol-1-yl)-N,N,N / ,N / -tetramethyluronium hexafluorophosphate
• HBTU O-Benzotriazol-1-yl-/V,N,N'.W-tetramethyluronium hexafluorophosphate
• MOM methoxymethyl
• PFU plaque forming units
• Ph phenyl
• RNAsin A ribonuclease inhibitor marketed by Promega Corporation
• TBE tris-borate-EDTA
• TBTU 2-( ⁇ H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; tBu: tert-butyl; TFA: trifluoroacetic acid;
• TFAA trifluoroacetic anhydride
• Tris 2-amino-2-hydroxymethyl-1 ,3-propanediol UMP: uridine 5'-monophosphate UTP: uridine 5'-triphosphate
• Examples 1-33 illustrate methods of synthesis of representative compounds of this invention.
• Methyl 3-amino-4-iodobenzoate 3-Amino-4-iodobenzoic acid (13.35 g, 50.8 mmol) was added to MeOH (150mL) and SOCI 2 (4.8 mL, 65.8 mmol, 1.3 equivalent) was added. The mixture was refluxed for 3 h and then volatiles were removed under reduced pressure. The residue was co- evaporated 3 x with MeOH and dried in vacuo (15.23 g).
• Methyl 3-trifluoroacetamido-4-iodobenzoate The aniline derivative from above (14.53 g, 52 mmol) was dissolved in DCM (200 mL) and TFAA (15 mL, 104 mmol) was added. The dark purple solution was refluxed overnight. Volatiles were removed under reduced pressure and the residue was passed through a short pad of silica gel using DCM as eluent. The desired product was obtained as a pink solid (13.81 g): MS (ES ' ) m/z 371.9 (M-H).
• Methyl 3-(cyclohexenyl)-2-phenylindole 6-carboxylate A flame-dried flask was charged with finely powdered anhydrous K 2 CO 3 (0.153 g, 1.1 mmol) and the alkyne derivative from above (0.390 g, 1.1 mmol). Dry DMF (4 mL) was added and the suspension degassed with a stream of argon. The enol triflate derived from cyclohexanone, prepared following the procedure described by A.G. Martinez, M. Hanack et al. (J. Heterocyclic Chem.
• a 12 L round-bottomed flask was equipped with a reflux condenser and a mechanical stirrer, and the system was purged with nitrogen gas.
• 6-indole carboxylic acid (300.00 g, 1.86 mole, 3 equivalents) was charged into the flask, followed by MeOH (5.5 L). After stirring for 10 min at room temperature, cyclohexanone (579 mL, 5.58 mole) was added.
• Methanolic sodium methoxide (25% w/w, 2.6 L, 11.37 mole, 6.1 equivalents) was added in portions over 10 min. The mixture was then refluxed for 48 h. After cooling to room temperature, water (4 L) was added and methanol removed under reduced pressure.
• Methyl 2-bromo-3-cyclohexyl-6-indole carboxyiate Adapting the procedure of L. Chu (Tet. Lett. 1997, 38, 3871) methyl 3-cyclohexyl-6- indole carboxyiate (4.65 g, 18.07 mmol) was dissolved in a mixture of THF (80 mL) and CHCI 3 (80 mL). The solution was cooled in an ice bath and pyridinium bromide perbromide (pyridine tribromide, 7.22 g, 22.6 mmol, 1.25 equivalent) was added. After stirring for 1.5 h at 0 °C, the reaction was judged complete by TLC.
• the precipitated potassium salt is collected by filtration, and washed with TBME (2 X 500 mL) to remove cyclopentanone self-condensation products.
• the brown solid was re-dissolved in water (2.5 L) and the solution washed with TBME (2 X 1 L).
• HCl 425 mL
• the beige precipitate was collected by filtration, washed with water (2 X 1 L) and dried under vacuum at 70 °C.
• the crude product weighed 275.9 g (88.9 % mass recovery) and had an homogeneity of 85% (HPLC).
• Methyl 3-cyclopentyl-6-indole carboxyiate The indole carboxylic acid from above was converted to the corresponding methyl ester using the carbonate / iodomethane procedure described in example 2.
• Methyl 2-bromo-3-cyclopentyl-6-indole carboxyiate The indole carboxyiate from above was brominated using pyridinium bromide perbromide following the procedure described in example 2.
• Cross-coupling of aromatic/heteroaromatic boronic acid or ester derivatives with 2- bromoindoles can be performed using any variations of the standard metal-catalyzed Suzuki cross-coupling reaction as described in the literature and well known to those skilled in the art.
• the following example serves to illustrate such a process and is non-limiting.
• Pd(PPh 3 ) 4 (3.06 g, 2.65 mmol, 0.1 equivalent) was added and the mixture stirred overnight at 75-85 °C under argon. Volatiles were removed under reduced pressure and the residue re-dissolved in EtOAc (500 mL). The solution was washed with water, saturated NaHCO 3 (100 mL) and brine (100 mL). After drying over a mixture of MgSO and decolorizing charcoal, the mixture was filtered and concentrated under reduced pressure.
• Methyl 1-carboxymethyl-3-cyclohexyl-2-furan-3-yl-1H-indole-6-carboxylate The tert-butyl ester from above (21.5 g, 49 mmol) was dissolved in dichloromethane (90 mL) and TFA (65.6 mL) was added dropwise to the solution which was stirred for 5 h at room temperature. Volatiles were removed under reduced pressure, the residue was co-evaporated 3 x with DCM and then dried under vacuum. The crude product was triturated with a mixture of hexane (200 mL) and DCM (20 mL), filtered and dried under vacuum to give the title compound of example 6 as a white solid (18.62 g, 99 % yield).
• the 2-bromoindole from example 2 was ⁇ /-alkylated with tert-butylbromoacetate using NaH in DMF and the tert-butyl ester cleaved with TFA as described in example 6 to give the title compound of example 8 as a white solid.
• the 2-bromoindole derivative from above (6.10 g, 13.54 mmol) was charged in a 100 mL flask equipped with a stirrer and reflux condenser. Anhydrous dioxane (50 mL) was added and tributyl(1-ethoxyvinyl)tin (6.27 g, 17.37 mmol, 1.2 equiv.) was added. The reaction mixture was degassed by bubbling argon through the suspension for 40 min. Dichlorobis(triphenylphosphine)palladium (0.51 g, 0.72 mmol) was added and the reaction mixture was stirred overnight at 100 °C under an argon atmosphere.
• X H, alkyl, NH 2 , NH(alkyl), NHCO(alkyl)
• the extract was washed with water, dried (MgSO ) and concentrated to give a residue that was purified by flash chromatography on silica gel using 15-20 % EtOAc in hexane as eluent.
• the methyl ester of example 13 was obtained as a light-yellow solid.
• the methyl ester from above (0.040 g, 0.095 mmol) was dissolved in a mixture of THF (3 mL) and MeOH (2 mL) and 2.5 N NaOH (400 ⁇ L) was added. The mixture was stirred at 50 °C for 5 h after which the reaction was judged complete by TLC. Volatiles were removed under reduced pressure and the residue was partitioned between 10 % aqueous HCl and DCM.
• the amide of example 9 (0.060 g, 0.137 mmol, 1 equiv.) was dissolved in THF (2 mL) and P 2 S 5 (0.031 g, 0.07 mmol, 0.51 equiv.) was added. The mixture was stirred at 50 °C for 15 h after which another portion of P 2 S 5 (0.020 g) was added. After stirring for an additional 2 h at 50 °C, the reaction mixture was concentrated under reduced pressure and the residue passed through a plug of silica gel using 60 % EtOAc in hexane + 3 % AcOH as eluent. The fractions containing the product were combined and after removal of solvents under reduced pressure, the residue was purified by preparative HPLC to give the title compound of example 14 as a white amorphous solid (11 mg).
• the crude methyl ester (540 mg, -2.2 mmol) and SnCI 2 dihydrate (2.25 g, 10 mmol) were dissolved in ethanol (20 mL) and the mixture was stirred at 80 °C for 4 hours. After that period, the mixture was cooled to room temperature and was slowly added to aqueous solution of saturated NaHCO 3 . The reaction mixture was extracted with ethyl acetate (100 mL), the organic layer was dried over anhydrous MgSO and the solvent was removed under reduced pressure.
• the amide was dissolved in acetic acid (10 mL) and stirred at 70 °C for 3 hours to induce dehydration and cyclization to the benzymidazole.
• the reaction mixture was concentrated to dryness, diluted with ethyl acetate (100 mL) and washed with 10% aqueous citric acid (2x), aqueous saturated NaHCO 3 and brine.
• the organic layer was dried over MgSO 4 , filtered and concentrated to dryness.
• the residue was purified by flash column chromatography, using a solvent gradient of hexane in ethyl acetate (from 80 % to 50 %), to give the SEM-protected benzymidazole intermediate as a pink solid (574 mg).
• R, R', R" are H or alkyl.
• R, R', R" are H or alkyl.
• Methyl 1 -(2-carboxy-ethyl)-3-cyclohexyl-2-furan-3-yl-1 H-indole-6-carboxylate The tert-butyl ester from above (40 mg) was dissolved in DCM (1 mL) and TFA (2 mL) was added. The mixture was stirred for 1 h at room temperature after which volatiles were removed under reduced pressure. The residue was co-evaporated twice with DCM and used as such in the next step.
• 2-aminoisobutyric acid was converted to the corresponding amino acid chloride hydrochloride: 2-oxazolidinone (12.30 g, 0.141 mole) was dissolved in MeCN (150 mL) and phosphorous pentachloride (49.02 g, 0.235 mole, 1.7 equivalent) was added in one portion. The homogeneous mixture was stirred for 24 h at room temperature. 2-Aminoisobutyric acid (14.55 g, 0.141 mole) was added and the suspension was stirred for 48 h at room temperature.
• the desired acid chloride hydrochloride was collected by filtration, washed with MeCN and dried under vacuum.
• Other , -disubstituted amino acid chloride hydrochlorides can be prepared in an analogous fashion starting from the corresponding amino acid (e.g. 1- aminocyclobutanecarboxylic acid, 1-aminocyclopentanecarboxylic acid, 1- aminocyclohexanecarboxylic acid and the like).
• the acid chloride (12.778 g, 80 mmol, 1.4 equivalent) was suspended in DCM (200 mL) and ethyl 4-aminocinnamate (11.045 g, 57.7 mmol, 1 equivalent) was added.
• the acid from above (0.519 g, 2.0 mmol) was dissolved in DCM (10 mL).
• DIEA (1.39 mL, 8.0 mmol, 4 equivalents) was added, followed by ethyl 4-aminocinnamate (0.573 g, 3.0 mmol, 1.5 equivalent) and HATU (1.143 g, 3.0 mmol, 1.5 equivalents).
• the mixture was stirred at room temperature for 3 days.
• the reaction was poured into TBME (100 mL) and the solution washed successively with 10% aqueous citric acid (2 x 25 mL) and saturated aqueous NaHCO 3 (25 mL), and dried over MgSO 4 .
• Diazomethane was slowly added to a solution of 4-chloro-3-nitrocinnamic acid in CH 3 OH/CH 2 CI 2 until the yellow color persisted, indicating the presence of excess diazomethane.
• the solution was evaporated to dryness under reduced pressure and the residue was dissolved in DMSO.
• the solution was heated to 140 °C and ammonia gas was bubbled through for a period of 4 hours.
• the mixture was cooled to room temperature and degassed with N 2 , and poured onto ice. The precipitate formed was filtered, washed with cold water and dried under vacuum for 16 hours to give the crude 4-amino-3-nitrocinnamic ester as a yellow solid (2.05 g).
• N-Fmoc-(3-N-Boc)-(S)-cucurbitine (0.495 g, 1.09 mmol), ethyl 4-aminocinnamate (0.300 g, 1.57 mmol), ⁇ OAt (0.224, 1.65 mmol) and ⁇ ATU (0.626 g, 1.65 mmol) were dissolved in DMF (7 mL). To this mixture, 2,4,6-collidine (0.435 mL, 3.30 mmol) was added and the solution was stirred at room temperature for 2 days.
• reaction mixture was poured into EtOAc (100 mL) and the solution washed successively with 10% aqueous citric acid (2 x 25 mL), saturated aqueous Na ⁇ CO 3 (25 mL) and brine (25 mL), and dried over anhydrous MgSO 4 .
• the solvent was removed under reduced pressure and the residue was dissolved in CH 2 CI 2 , DBU (0.658 mL, 4.4 mmol) was added and the reaction mixture was stirred at room temperature for 15 hours.
• N-Fmoc-amino-(3-N-Boc-piperidinyl)carboxylic acid was coupled to the ethyl ester of 4-aminocinnamic acid using HATU / HOAT / collidine in DMF and the Fmoc protecting group was. removed with piperidine to give the title compound of example 24 in racemic form.
• Racemic N-Fmoc-amino-(3-N-Boc-piperidinyl)carboxylic acid could also be resolved into its two enantiomers by preparative HPLC on a chiral support (Chiralcel OD, 10 micron, 2.00 cm I.D. x 25 cm), using 35% H 2 O in MeCN as the eluent. Enantiomeric amines could then be coupled to indole carboxylic acids to prepare enantiomerically pure inhibitors.
• the Boc-protected bromoaniline (10.7 g, 39.2 mmol) was dissolved in anhydrous THF (75 mL) in a flask equipped with an overhead stirrer. The solution was cooled to 0 °C and MeLi (1.2 M in Et 2 O, 33 m ' L, 39.2 mmol) was added drop wise while maintaining the internal temperature below 7 °C. The reaction mixture was stirred at 0 °C for 15 min and then cooled to -78 °C before n-BuLi (2.4 M in hexane, 17 mL, 39.2 mmol) was added drop wise, maintaining the internal temperature below -70 °C).
• reaction mixture was stirred at -78 °C for 1 h, B(OEt) 3 (17 mL, 98 mmol) was added drop wise (internal temperature ⁇ -65 °C) and stirring was continued for 45 min at -78 °C and at 0 °C for 1 h.
• the reaction mixture was then treated with 5% aqueous HCl (-100 mL, to pH ⁇ 1) for 15 min and NaCI(s) was added to saturate the aqueous layer.
• the aqueous layer was extracted with 0.5 M NaOH (4 x 100 mL) and the combined aqueous layers were acidified with 5% HCl (150 mL, to pH ⁇ 1 ) and extracted with Et 2 O (3 x 200 mL). The combined organic layers were dried over anhydrous MgSO 4 , filtered and concentrated to give the N-Boc carbamate of 4-aminophenylboronic acid as a solid (7.5 g).
• the carbamate-ester product was isolated after flash column chromatography using 20% to 30% EtOAc in hexane: 180 mg.
• the aniline hydrochloride of example 26 was isolated after removal of the Boc protecting group with 4N HCl in dioxane for 30 min.
• the ethyl ester of 5-nitroindole-2-carboxylic acid (0.300 g, 1.28 mmol) was dissolved in anhydrous DMF (6 mL) and NaH (0.078 g, 60%, 1.92 mmol) was added. The reaction was stirred at RT for 20 min, then Mel (160 ⁇ L, 2.56 mmol) was added and stirring was continued for 3 h. The reaction was quenched with the addition of aqueous NaHCO 3 (-1%) while stirring vigorously. The brown solid formed (0.096 g) was filtered and dried in air overnight.
• the 5-aminoindole derivative of example 27 was coupled to N-Fmoc-amino-(4-N- Boc-piperidinyl)carboxylic acid.
• the Boc protecting group was removed with 25% TFA in CH 2 CI 2 in the usual way, and the product was then dissolved in EtOH (6 mL).
• AcOH (133 mg), acetaldehyde (33 mg, 0.74 mmol) and NaCNBH 3 (23mg, 0.37 mmol) were added and the reaction mixture was stirred at room temperature for 2 h.
• the reaction mixture was concentrated to remove most of the solvent, the residue was re-dissolved in EtOAc and washed with saturated NaHCO 3 and brine.
• the organic layer was dried over anhydrous MgSO 4 and concentrated to give the N-ethyl derivative as an orange solid.
• Indole carboxylic acids were coupled to various amines (for example according to the examples 15a, 15b, 15c, 19, 20, 21 , 22, 23, 24, 25, 28, 34, 35, 36, 42, 43, or 45) using standard amide bond forming procedures familiar to those skilled in the art.
• Amide bond forming reagents include but are not limited to carbodiimides (DCC, EDC), TBTU, HBTU, HATU and BOP-CI in the presence or absence of additives such as HOBt or HOAT.
• Indole carboxylic acids can also be activated for coupling by conversion to the corresponding acid chloride, symmetrical anhydride or unsymmetrical anhydrides using standard protocols familiar to those skilled in the art of organic chemistry.
• indole carboxylic acids with amines is generally carried out in solvents such as THF, DCM, DMF, DMSO or MeCN, in the presence of a tertiary organic base including, but not limited to triethylamine, N- methylmorpholine, collidine and dusopropylethylamine.
• solvents such as THF, DCM, DMF, DMSO or MeCN
• a tertiary organic base including, but not limited to triethylamine, N- methylmorpholine, collidine and dusopropylethylamine.
• Indole carboxylic acids were converted to the corresponding acid chloride and coupled to various sulfonamides in the presence of DMAP and an organic base such as triethylamine, DIEA, /V-methylmorpholine and the like.
• the carboxylic acid was activated using amide bond forming agents such as carbodiimides (DCC, EDC), TBTU, HATU and the like and treated with sulfonamides in the presence of DMAP.
• Sulfonamides were either from commercial sources or prepared from the corresponding sulfonyl chlorides and a solution of ammonia in dioxane.
• ⁇ /-methylacylsulfonamide of example 31 was prepared from the acid chloride described in example 30 and ⁇ /-methylbenzenesulfonamide using the procedure of example 30.
• Methyl 4-hydroxybenzoate (20.00 g, 131 mmol) was dissolved in DMF (350 mL) and K 2 CO 3 (24.19 g, 175 mmol) was added. The mixture was stirred for 30 min and crotyl bromide (85%, 16.47 mL, 160 mmol) was added dropwise over 4 min. The resulting amber suspension was stirred for 4 h at room temperature. It was then poured into DCM and the solution washed with water and brine. The extract was dried (MgSO 4 ) and evaporated to a pale yellow oil consisting of a mixture of two isomeric allyl ether (4:1 ratio). Upon standing at room temperature, the oil partially crystallized. The supernatant was decanted and the crystals washed with hexane to provide 12.5 g of the desired ether as white crystals.
• the crude product which consists of a mixture of aldehyde and lactol was obtained as a milky oil (9.9 g).
• the crude product from above (9.9 g, 48 mmol) was suspended in 85% phosphoric acid (40 mL) and heated to 50 °C for 50 min after which a white solid precipitated.
• Water (50 mL) was added and the solid collected by filtration. The material was then dissolved in EtOAc and washed with saturated aqueous NaHCO 3 and water.
• Indole 6-carboxylic acid (10.00 g, 62 mmol) was esterified by refluxing overnight in a mixture of MeOH (200 mL) and cone. H 2 SO 4 (1 mL). After cooling, the reaction mixture was poured into sat. aqueous NaHCO 3 and extracted with EtOAc. The extract was washed with aqueous NaHC0 3 twice and water. Drying (MgS0 ) and removal of volatiles gave the desired methyl ester as a brown oil (10.4 g). The ester from above (10.40 g, 62 mmol) was dissolved in DMF (80 mL) and the solution cooled in ice.
• the cinnamate derivative from above (0.400 g, 0.9 mmol) was dissolved in CHCI 3 (15 mL) and sodium azide (138 mg, 2.1 mmol) was added. TFA (0.39 mL, 5.1 mmol) was added dropwise over 5 min and the mixture was then stirred at 60 °C for 4 h.
• the reaction mixture was diluted with CHCI 3 , washed with aqueous NaHCO 3 and dried (MgSO ).
• the product was purified by flash chromatography on silica gel using 20% EtOAc in hexane as eluent, to give the desired azide as a yellow foam (0.207
• the ortho-ethoxy-para-nitro cinnamate derivative prepared as described in example 36 (600 mg; 2.39 mmol) was dissolved in concentrated sulphuric acid (5.5 mL) at 0°C and potassium nitrate (253 mg; 2.50 mmol) added in portions over 3 min. After 5 min, the resulting yellow-brown solution was allowed to warm to ambient temperature and was stirred under a nitrogen atmosphere. After 3 h, the reaction was added to ice (75 g) resulting in a pale yellow precipitate. Once the ice had melted, the suspension was sonicated, filtered and washed several times with distilled water.
• analogs of derivatives presented in examples 36 and 37 where the alkoxy group has been replaced by an alkyl, alkenyl or alkynyl substitutent can be prepared by converting such an alkoxy derivative (e.g. methoxy) to the corresponding phenol by cleaving the ether linkage with reagents such as BBr 3 and then converting the phenol substituent to the corresponding triflate.
• Such triflates can then be used as substrates in a variety of transition metal catalyzed cross-coupling reactions with organometallic reagents that would allow replacement of the triflate functionality by an alkyl substituent.
• Such reagents might include tetraalkyltin, tetraalkenyltin, alkylboronic acid and alkenylboronic acid derivatives that would undergo cross-coupling under Pd° catalysis.
• the substituent can be further elaborated (e.g. the double bond can be converted to a cyclopropane ring using a cyclopropanating reagent known to people skilled in the art)
• the alkyl group has been introduced, the intermediates can then be elaborated to inhibitors following synthetic sequences described in previous examples.
• Step 1 3-amino-4-methylbenzoic acid (15.00 g, 0.099 mol) was suspended in MeOH (150 mL) and thionyl chloride (25.33 mL, 0.347 mol, 3.5 equiv.) was added dropwise. The mixture was heated overnight at 70 °C. After cooling to RT, volatiles were removed under reduced pressure and the residue triturated with ether (150 mL). The solid was filtered off and dried (18.36 g). The solid was suspended in DCM (600 mL) and saturated aqueous NaHC0 3 (250 mL) was added.
• Steps 2 and 3 the ester from above (12.50 g, 75.6 mmol) was dissolved in DCM (190 mL) and methylthioaldehyde dimethyl acetal (10.1 mL, 75.6 mmol) was added. The solution was cooled to -30 °C. N-chlorosuccinimide (10.10 g, 75.6 mmol) was added in 6 portions over 30 minutes. Triethylamine (10.6 mL, 75.6 mmol) was then added dropwise over 10 min and after stirring for an additional 15 min, the cooling bath was removed and the temperature brought to reflux. After 5 h, the reaction mixture was cooled to RT and evaporated to dryness.
• Step 4 the thiomethyl indole from above (8.37 g, 35.4 mmol) was dissolved in absolute EtOH (220 mL) and Raney-nickel (Ra-Ni) (25 g) was added. After stirring at RT for 3 h, another portion of Ra-Ni (15 g) was added and stirring resumed for an additional 45 min. The mixture was filtered and the filtrate evaporated to dryness to give the desired indole (6.26 g, 93%).
• Ra-Ni Raney-nickel
• Steps 5 the indole ester from above (4.00 g, 21 mmol) was dissolved in a mixture of MeOH (18 mL) and water (18 mL). KOH (11.86 g, 210 mmol) was added and the mixture stirred at 75 °C for 2 h. Cyclohexanone (7.26 g, 74 mmol, 3 equiv.) was added dropwise over 15 min and stirring at 75 °C was continued overnight. MeOH was removed under reduced pressure and water (500 mL) was added to the residue. Insoluble material was removed by filtration and the aqueous phase was then washed with TBME (200 mL).
• aqueous phase was acidified to pH 4 with formic acid to produce a white precipitate that was collected by filtration, washed with water and dried.
• the desired cyclohexenylindole was obtained (4.77 g, 89%).
• Steps 6-8 as described in example 2.
• Steps 9-11 as described in examples 4 and 6..
• Step 1 4-methylsalicylic acid (100 g, 0.66 mol) was dissolved in acetone (1 L) and K 2 C0 3 (227 g, 1.64 mol, 2.5 equiv.) was added in portions. The mixture was heated to reflux and dimethylsulfate (155 mL, 1.64 mol, 2.5 equiv.) was added dropwise over 1 h. The mixture was refluxed overnight. Additional K 2 CO 3 (90 g) and dimethylsulfate (60 mL) were added and the mixture refluxed for an additional 20 h. K 2 C0 3 (20 g) and dimethylsulfate (15 mL) were again added and after refluxing for 7 h, the reaction was judged complete by TLC.
• Step 2 the ester from above (117 g, 0.649 mol) was charged in a flask cooled in ice. The ester was dissolved in cone. H S0 4 (600 mL) and the solution cooled to -3 °C.
• Step 4 The enamine from step 3 (90.02 g, 0.321 mol) was dissolved in 1 :1 THF- MeOH (1.48 L) and the mixture heated to 35 °C in a water bath. Raney nickel (washed with THF, 6.3 g) was added followed by dropwise addition of hydrazine (18.5 g, 0.369 mol) over 15 min. After stirring for 1 h (internal temperature: 49 °C), a second portion of hydrazine (18.5 g) was added dropwise and the mixture stirred overnight at 49 °C.
• Step 1 The starting protected amino acid was obtained using a similar procedure to that described in example 21 but using benzyl alcohol instead of trimethylsilyl ethanol in the curtius rearrangement.
• the acid (7.48 g, 30mmol) was dissolved in THF (50 mL) and the solution cooled to -8 °C under a nitrogen atmosphere.
• N- Methylmorpholine (3.63 mL, 33 mmol) was added dropwise followed by isobutylchloroformate (3.89 mL, 30 mmol). The suspension was stirred for 10 min and filtered under nitrogen, keeping the filtrate at -8 °C.
• Step 2 The bromomethylketone from above (228 mg, 0.7 mmol) and thioacetamide (56.3 mg, 0.75 mmol) were heated to reflux in isopr ⁇ panol (5 mL). After 1 h, the reaction mixture was evaporated to dryness and the oily residue triturated with water to give a white precipitate that was collected, washed with water and dried in vacuum (185 mg, 87% yield).
• Step 3 10% Pd on charcoal (70 mg) was suspended in EtOH (5 mL) and the protected thiazole derivative from above (180 mg) was added. Hydrochloric acid was added to acidify the reaction mixture which was then stirred under 1 atm of H 2 gas for 20 h. The catalyst was removed by filtration and the filtrate evaporated to dryness under reduced pressure to give the desired amine hydrochloride as a white solid (104 mg) after trituration with ether. The amine hydrochloride was coupled to indole derivatives under standard conditions.
• Analogous thiazole derivatives can be prepared in a similar way by using differently substituted thioamide, thiourea or acylthiourea derivatives.
• other protected amino acids can be used as starting materials in this sequence and converted to their respective bromo or chloromethylketones to be used in turn to prepare various substituted thiazole derivatives.
• the 4-nitro-2-ethoxycinnamate (303 mg, 1.206 mmol), prepared as described in example 36 was dissolved in concentrated sulfuric acid ( 3 mL) and the solution cooled to 0 °C. Potassium nitrate (128 mg, 1.27 mmol) was added and the mixture stirred for 3.5 h at room temperature. After completion, the reaction mixture was poured over ice and the precipitated solid was collected by filtration. The crude product was washed with water, dried under vacuum and used without purification in the next step (390 mg).
• the dinitro derivative from above (390 mg) was dissolved in THF (3 mL) and methylamine in THF (3.02 mL of a 2M solution in THF) was added.
• Step 1 4-methylsalicylic acid (32.1 g, 0.21 mol) and potassium carbonate (61.2 g, 0.44 mol) were suspended in acetone (300 mL) and the mixture brought to reflux temperature. Dimethyl sulfate (66.5 g, 0.53 mol) was added dropwise within 1 h and stirring continued overnight at reflux. Additional dimethylsulfate (30 mL) and potassium carbonate (2 X 15 g) were added and refluxing for an additional 24 h was required to complete the reaction. The reaction mixture was then cooled to room temperature and inorganic salts removed by filtration using acetone for washings. The filtrate was evaporated under reduced pressure and the oily residue was dissolved in MeOH (300 mL).

Landscapes

• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Pharmacology & Pharmacy (AREA)
• General Chemical & Material Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Virology (AREA)
• Communicable Diseases (AREA)
• Engineering & Computer Science (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Oncology (AREA)
• Molecular Biology (AREA)
• Gastroenterology & Hepatology (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Plural Heterocyclic Compounds (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
• Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
• Hydrogenated Pyridines (AREA)
• Indole Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Priority Applications (13)

Applications Claiming Priority (2)

Publications (2)

Family

ID=32771985

Family Applications (1)

Country Status (25)

Cited By (91)

Families Citing this family (40)

Citations (5)

Family Cites Families (98)

• 2004
  • 2004-01-12 US US10/755,256 patent/US7223785B2/en active Active
  • 2004-01-19 MX MXPA05007754A patent/MXPA05007754A/es active IP Right Grant
  • 2004-01-19 EP EP04703130A patent/EP1587787A1/en not_active Withdrawn
  • 2004-01-19 KR KR1020057013544A patent/KR20050095863A/ko not_active Application Discontinuation
  • 2004-01-19 NZ NZ541852A patent/NZ541852A/en unknown
  • 2004-01-19 PL PL378194A patent/PL378194A1/pl not_active Application Discontinuation
  • 2004-01-19 CN CNA2004800078316A patent/CN1764641A/zh active Pending
  • 2004-01-19 BR BR0406926-9A patent/BRPI0406926A/pt not_active IP Right Cessation
  • 2004-01-19 RS YUP-2005/0556A patent/RS20050556A/sr unknown
  • 2004-01-19 EA EA200501065A patent/EA009323B1/ru not_active IP Right Cessation
  • 2004-01-19 WO PCT/CA2004/000018 patent/WO2004065367A1/en active Search and Examination
  • 2004-01-19 CA CA2511307A patent/CA2511307C/en not_active Expired - Fee Related
  • 2004-01-19 AU AU2004205429A patent/AU2004205429A1/en not_active Abandoned
  • 2004-01-19 UA UAA200508155A patent/UA83651C2/ru unknown
  • 2004-01-19 JP JP2006500429A patent/JP4585507B2/ja not_active Expired - Fee Related
  • 2004-01-20 CL CL200400076A patent/CL2004000076A1/es unknown
  • 2004-01-20 PE PE2004000084A patent/PE20040940A1/es not_active Application Discontinuation
  • 2004-01-20 TW TW093101632A patent/TW200418843A/zh unknown
  • 2004-01-21 AR ARP040100155A patent/AR047754A1/es unknown
• 2005
  • 2005-06-15 ZA ZA200504893A patent/ZA200504893B/en unknown
  • 2005-07-11 EC EC2005005913A patent/ECSP055913A/es unknown
  • 2005-07-20 IL IL169777A patent/IL169777A0/en unknown
  • 2005-07-21 HR HR20050662A patent/HRP20050662A2/xx not_active Application Discontinuation
  • 2005-08-19 NO NO20053892A patent/NO20053892L/no not_active Application Discontinuation
  • 2005-08-22 CO CO05083254A patent/CO5590912A2/es not_active Application Discontinuation
• 2007
  • 2007-02-07 US US11/672,293 patent/US7888363B2/en active Active
• 2009
  • 2009-11-11 JP JP2009258002A patent/JP2010077139A/ja not_active Abandoned

Patent Citations (5)

Non-Patent Citations (1)